SomamiR DB 2.0
Somatic mutations altering microRNA-ceRNA interactions
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PolymiRTS Database
Prediction criteria: TargetScan sites only     All 6mer or longer seed matches
Transcript ID: NM_052907
Gene Symbol: TMEM132B
Browse Associations

Somatic mutations that impact miRNA target sites


Mutation Mutation ID Sample Name Cancer Type
chr12:g.125654536G>A COSM692360 TCGA-DA-A3F8-06 [skin][NS][malignant_melanoma][NS]
miRNA Targets Table
miR ID miRSite miRSeed SeedClass FuncClass Cluster ID
hsa-miR-130b-5p caaagaGAAAGAGag ACUCUUUC m7b Created HHHSE_19037_TMEM132B|NM_052907|exon_CDS|-4.50659824857872|1.21971031976463
hsa-miR-1238-3p caaaGAGGAAGagag CUUCCUCG m7a Disrupted HHHSE_19037_TMEM132B|NM_052907|exon_CDS|-4.50659824857872|1.21971031976463
hsa-miR-1236-3p caaagaGGAAGAGag CCUCUUCC m7b Disrupted HHHSE_19037_TMEM132B|NM_052907|exon_CDS|-4.50659824857872|1.21971031976463
hsa-miR-877-3p caAAGAGGAagagag UCCUCUUC m7a (m7a->m6a) HHHNE_19037_TMEM132B|NM_052907|exon_CDS|-4.50659824857872|1.21971031976463
hsa-miR-7111-3p caaAGAGGAagagag AUCCUCUC m6b Disrupted HHHNE_19037_TMEM132B|NM_052907|exon_CDS|-4.50659824857872|1.21971031976463
hsa-miR-6881-3p caAAGAGGAagagag AUCCUCUU m7b (m7b->m6b) HHHNE_19037_TMEM132B|NM_052907|exon_CDS|-4.50659824857872|1.21971031976463
hsa-miR-6809-3p caAAGAGAAagagag CUUCUCUU m7b (m6b->m7b) HHHNE_19037_TMEM132B|NM_052907|exon_CDS|-4.50659824857872|1.21971031976463
hsa-miR-6780a-3p caaAGAGGAagagag CUCCUCUG m6b Disrupted HHHNE_19037_TMEM132B|NM_052907|exon_CDS|-4.50659824857872|1.21971031976463
hsa-miR-6809-3p caAAGAGAAagagag CUUCUCUU m7b (m6b->m7b) HHHSE_19037_TMEM132B|NM_052907|exon_CDS|-4.50659824857872|1.21971031976463
hsa-miR-877-3p caAAGAGGAagagag UCCUCUUC m7a (m7a->m6a) HHHSE_19037_TMEM132B|NM_052907|exon_CDS|-4.50659824857872|1.21971031976463
hsa-miR-7111-3p caaAGAGGAagagag AUCCUCUC m6b Disrupted HHHSE_19037_TMEM132B|NM_052907|exon_CDS|-4.50659824857872|1.21971031976463
hsa-miR-6881-3p caAAGAGGAagagag AUCCUCUU m7b (m7b->m6b) HHHSE_19037_TMEM132B|NM_052907|exon_CDS|-4.50659824857872|1.21971031976463
hsa-miR-6780a-3p caaAGAGGAagagag CUCCUCUG m6b Disrupted HHHSE_19037_TMEM132B|NM_052907|exon_CDS|-4.50659824857872|1.21971031976463
hsa-miR-4768-5p caaAGAGAAagagag AUUCUCUC m6b Created HHHSE_19037_TMEM132B|NM_052907|exon_CDS|-4.50659824857872|1.21971031976463
hsa-miR-4753-3p cAAAGAGAAagagag UUCUCUUU m8a (m7a->m8a) HHHSE_19037_TMEM132B|NM_052907|exon_CDS|-4.50659824857872|1.21971031976463
hsa-miR-1236-3p caaagaGGAAGAGag CCUCUUCC m7b Disrupted HHHNE_19037_TMEM132B|NM_052907|exon_CDS|-4.50659824857872|1.21971031976463
hsa-miR-1238-3p caaaGAGGAAGagag CUUCCUCG m7a Disrupted HHHNE_19037_TMEM132B|NM_052907|exon_CDS|-4.50659824857872|1.21971031976463
hsa-miR-130b-5p caaagaGAAAGAGag ACUCUUUC m7b Created HHHNE_19037_TMEM132B|NM_052907|exon_CDS|-4.50659824857872|1.21971031976463
hsa-miR-4753-3p cAAAGAGAAagagag UUCUCUUU m8a (m7a->m8a) HHHNE_19037_TMEM132B|NM_052907|exon_CDS|-4.50659824857872|1.21971031976463
hsa-miR-4768-5p caaAGAGAAagagag AUUCUCUC m6b Created HHHNE_19037_TMEM132B|NM_052907|exon_CDS|-4.50659824857872|1.21971031976463

Mutation Mutation ID Sample Name Cancer Type
chr12:g.125654528C>A COSM1511260 TCGA-95-7043-01 [lung][right_upper_lobe][carcinoma][adenocarcinoma]
miRNA Targets Table
miR ID miRSite miRSeed SeedClass FuncClass Cluster ID
hsa-miR-296-5p ttcGGGCCCaaagag AGGGCCCC m6b Disrupted HHHSE_19037_TMEM132B|NM_052907|exon_CDS|-4.50659824857872|1.21971031976463
hsa-miR-2113 ttcggGCACAAAgag AUUUGUGC m7b Created HHHSE_19037_TMEM132B|NM_052907|exon_CDS|-4.50659824857872|1.21971031976463
hsa-miR-550b-2-5p ttcgGGCACAaagag AUGUGCCU m6b Created HHHSE_19037_TMEM132B|NM_052907|exon_CDS|-4.50659824857872|1.21971031976463
hsa-miR-6724-5p ttcGGGCCCAaagag CUGGGCCC m7b Disrupted HHHSE_19037_TMEM132B|NM_052907|exon_CDS|-4.50659824857872|1.21971031976463
hsa-miR-6773-5p ttcGGGCCCAAagag UUGGGCCC m8a Disrupted HHHSE_19037_TMEM132B|NM_052907|exon_CDS|-4.50659824857872|1.21971031976463
hsa-miR-6844 ttcgggcACAAAGAg UUCUUUGU m7b Created HHHSE_19037_TMEM132B|NM_052907|exon_CDS|-4.50659824857872|1.21971031976463
hsa-miR-2113 ttcggGCACAAAgag AUUUGUGC m7b Created HHHNE_19037_TMEM132B|NM_052907|exon_CDS|-4.50659824857872|1.21971031976463
hsa-miR-296-5p ttcGGGCCCaaagag AGGGCCCC m6b Disrupted HHHNE_19037_TMEM132B|NM_052907|exon_CDS|-4.50659824857872|1.21971031976463
hsa-miR-550b-2-5p ttcgGGCACAaagag AUGUGCCU m6b Created HHHNE_19037_TMEM132B|NM_052907|exon_CDS|-4.50659824857872|1.21971031976463
hsa-miR-6724-5p ttcGGGCCCAaagag CUGGGCCC m7b Disrupted HHHNE_19037_TMEM132B|NM_052907|exon_CDS|-4.50659824857872|1.21971031976463
hsa-miR-6773-5p ttcGGGCCCAAagag UUGGGCCC m8a Disrupted HHHNE_19037_TMEM132B|NM_052907|exon_CDS|-4.50659824857872|1.21971031976463
hsa-miR-6844 ttcgggcACAAAGAg UUCUUUGU m7b Created HHHNE_19037_TMEM132B|NM_052907|exon_CDS|-4.50659824857872|1.21971031976463

Mutation Mutation ID Sample Name Cancer Type
chr12:g.125654524G>A COSM4166098 C0052T [kidney][NS][other][neoplasm]
miRNA Targets Table
miR ID miRSite miRSeed SeedClass FuncClass Cluster ID
hsa-miR-2861 attcttCAGGCCCaa GGGGCCUG m7b Created HHHNE_19037_TMEM132B|NM_052907|exon_CDS|-4.50659824857872|1.21971031976463
hsa-miR-296-5p attcttcGGGCCCaa AGGGCCCC m6b Disrupted HHHNE_19037_TMEM132B|NM_052907|exon_CDS|-4.50659824857872|1.21971031976463
hsa-miR-4671-5p atTCTTCGGgcccaa ACCGAAGA m7b (m7b->m6b) HHHNE_19037_TMEM132B|NM_052907|exon_CDS|-4.50659824857872|1.21971031976463
hsa-miR-6724-5p attcttcGGGCCCAa CUGGGCCC m7b Disrupted HHHNE_19037_TMEM132B|NM_052907|exon_CDS|-4.50659824857872|1.21971031976463
hsa-miR-6773-5p attcttcGGGCCCAa UUGGGCCC m7b Disrupted HHHNE_19037_TMEM132B|NM_052907|exon_CDS|-4.50659824857872|1.21971031976463
hsa-miR-2861 attcttCAGGCCCaa GGGGCCUG m7b Created HHHSE_19037_TMEM132B|NM_052907|exon_CDS|-4.50659824857872|1.21971031976463
hsa-miR-296-5p attcttcGGGCCCaa AGGGCCCC m6b Disrupted HHHSE_19037_TMEM132B|NM_052907|exon_CDS|-4.50659824857872|1.21971031976463
hsa-miR-4671-5p atTCTTCGGgcccaa ACCGAAGA m7b (m7b->m6b) HHHSE_19037_TMEM132B|NM_052907|exon_CDS|-4.50659824857872|1.21971031976463
hsa-miR-6724-5p attcttcGGGCCCAa CUGGGCCC m7b Disrupted HHHSE_19037_TMEM132B|NM_052907|exon_CDS|-4.50659824857872|1.21971031976463
hsa-miR-6773-5p attcttcGGGCCCAa UUGGGCCC m7b Disrupted HHHSE_19037_TMEM132B|NM_052907|exon_CDS|-4.50659824857872|1.21971031976463

Mutation Mutation ID Sample Name Cancer Type
chr12:g.125654520C>T COSM1746832 B34-Tumor [urinary_tract][bladder][carcinoma][NS]
miRNA Targets Table
miR ID miRSite miRSeed SeedClass FuncClass Cluster ID
hsa-miR-4671-5p atgaatTCTTCGGgc ACCGAAGA m7b Disrupted HHHNE_19037_TMEM132B|NM_052907|exon_CDS|-4.50659824857872|1.21971031976463
hsa-miR-4760-3p ATGAATTTttcgggc AAAUUCAU m8a Created HHHNE_19037_TMEM132B|NM_052907|exon_CDS|-4.50659824857872|1.21971031976463
hsa-miR-4671-5p atgaatTCTTCGGgc ACCGAAGA m7b Disrupted HHHSE_19037_TMEM132B|NM_052907|exon_CDS|-4.50659824857872|1.21971031976463
hsa-miR-4760-3p ATGAATTTttcgggc AAAUUCAU m8a Created HHHSE_19037_TMEM132B|NM_052907|exon_CDS|-4.50659824857872|1.21971031976463

Mutation Mutation ID Sample Name Cancer Type
chr12:g.125654515G>T COSM936839 TCGA-BS-A0UF-01 [endometrium][NS][carcinoma][endometrioid_carcinoma]
miRNA Targets Table
miR ID miRSite miRSeed SeedClass FuncClass Cluster ID
hsa-miR-376a-3p aacCTATGAattctt AUCAUAGA m6b Disrupted HHHNE_19037_TMEM132B|NM_052907|exon_CDS|-4.50659824857872|1.21971031976463
hsa-miR-376b-3p aacCTATGAattctt AUCAUAGA m6b Disrupted HHHNE_19037_TMEM132B|NM_052907|exon_CDS|-4.50659824857872|1.21971031976463
hsa-miR-4760-3p aacctATGAATTctt AAAUUCAU m7b Disrupted HHHNE_19037_TMEM132B|NM_052907|exon_CDS|-4.50659824857872|1.21971031976463
hsa-miR-633 aacCTATTAattctt CUAAUAGU m6b Created HHHNE_19037_TMEM132B|NM_052907|exon_CDS|-4.50659824857872|1.21971031976463
hsa-miR-376a-3p aacCTATGAattctt AUCAUAGA m6b Disrupted HHHSE_19037_TMEM132B|NM_052907|exon_CDS|-4.50659824857872|1.21971031976463
hsa-miR-376b-3p aacCTATGAattctt AUCAUAGA m6b Disrupted HHHSE_19037_TMEM132B|NM_052907|exon_CDS|-4.50659824857872|1.21971031976463
hsa-miR-4760-3p aacctATGAATTctt AAAUUCAU m7b Disrupted HHHSE_19037_TMEM132B|NM_052907|exon_CDS|-4.50659824857872|1.21971031976463
hsa-miR-633 aacCTATTAattctt CUAAUAGU m6b Created HHHSE_19037_TMEM132B|NM_052907|exon_CDS|-4.50659824857872|1.21971031976463

Mutation Mutation ID Sample Name Cancer Type
chr12:g.125654515G>A COSM4406277 TCGA-D9-A6EC-06 [skin][NS][malignant_melanoma][NS]
miRNA Targets Table
miR ID miRSite miRSeed SeedClass FuncClass Cluster ID
hsa-miR-376a-3p aacCTATGAattctt AUCAUAGA m6b Disrupted HHHNE_19037_TMEM132B|NM_052907|exon_CDS|-4.50659824857872|1.21971031976463
hsa-miR-376b-3p aacCTATGAattctt AUCAUAGA m6b Disrupted HHHNE_19037_TMEM132B|NM_052907|exon_CDS|-4.50659824857872|1.21971031976463
hsa-miR-4760-3p aacctATGAATTctt AAAUUCAU m7b Disrupted HHHNE_19037_TMEM132B|NM_052907|exon_CDS|-4.50659824857872|1.21971031976463
hsa-miR-376a-3p aacCTATGAattctt AUCAUAGA m6b Disrupted HHHSE_19037_TMEM132B|NM_052907|exon_CDS|-4.50659824857872|1.21971031976463
hsa-miR-376b-3p aacCTATGAattctt AUCAUAGA m6b Disrupted HHHSE_19037_TMEM132B|NM_052907|exon_CDS|-4.50659824857872|1.21971031976463
hsa-miR-4760-3p aacctATGAATTctt AAAUUCAU m7b Disrupted HHHSE_19037_TMEM132B|NM_052907|exon_CDS|-4.50659824857872|1.21971031976463

Mutation Mutation ID Sample Name Cancer Type
chr12:g.125654513A>G COSM3384137 8034252 [pancreas][NS][carcinoma][NS]
miRNA Targets Table
miR ID miRSite miRSeed SeedClass FuncClass Cluster ID
hsa-miR-376a-3p tgaacCTATGAattc AUCAUAGA m6b Disrupted HHHNE_19037_TMEM132B|NM_052907|exon_CDS|-4.50659824857872|1.21971031976463
hsa-miR-376b-3p tgaacCTATGAattc AUCAUAGA m6b Disrupted HHHNE_19037_TMEM132B|NM_052907|exon_CDS|-4.50659824857872|1.21971031976463
hsa-miR-4760-3p tgaacctATGAATTc AAAUUCAU m7b Disrupted HHHNE_19037_TMEM132B|NM_052907|exon_CDS|-4.50659824857872|1.21971031976463
hsa-miR-513a-5p tgaaCCTGTGAAttc UUCACAGG m8a Created HHHNE_19037_TMEM132B|NM_052907|exon_CDS|-4.50659824857872|1.21971031976463
hsa-miR-376a-3p tgaacCTATGAattc AUCAUAGA m6b Disrupted HHHSE_19037_TMEM132B|NM_052907|exon_CDS|-4.50659824857872|1.21971031976463
hsa-miR-376b-3p tgaacCTATGAattc AUCAUAGA m6b Disrupted HHHSE_19037_TMEM132B|NM_052907|exon_CDS|-4.50659824857872|1.21971031976463
hsa-miR-4760-3p tgaacctATGAATTc AAAUUCAU m7b Disrupted HHHSE_19037_TMEM132B|NM_052907|exon_CDS|-4.50659824857872|1.21971031976463
hsa-miR-513a-5p tgaaCCTGTGAAttc UUCACAGG m8a Created HHHSE_19037_TMEM132B|NM_052907|exon_CDS|-4.50659824857872|1.21971031976463

Mutation Mutation ID Sample Name Cancer Type
chr12:g.125650725G>T COSM4530165 CSCC-41-T [skin][head_neck][carcinoma][squamous_cell_carcinoma]
miRNA Targets Table
miR ID miRSite miRSeed SeedClass FuncClass Cluster ID
hsa-miR-1248 agAAGAAGGgacgag ACCUUCUU m7b (m7b->m6b) HHHNA_6258_TMEM132B|NM_052907|exon_CDS|-0.874998545922905|-0.20274186935389
hsa-miR-4778-3p aGAAGAAGggacgag UCUUCUUC m7b Disrupted HHHNA_6258_TMEM132B|NM_052907|exon_CDS|-0.874998545922905|-0.20274186935389
hsa-miR-5088-3p agaAGAAGGGAcgag UCCCUUCU m8a Disrupted HHHNA_6258_TMEM132B|NM_052907|exon_CDS|-0.874998545922905|-0.20274186935389
hsa-miR-1248 agAAGAAGGgacgag ACCUUCUU m7b (m7b->m6b) HHHNE_19036_TMEM132B|NM_052907|exon_CDS|-0.919987936338531|-0.371790509209006
hsa-miR-4778-3p aGAAGAAGggacgag UCUUCUUC m7b Disrupted HHHNE_19036_TMEM132B|NM_052907|exon_CDS|-0.919987936338531|-0.371790509209006
hsa-miR-5088-3p agaAGAAGGGAcgag UCCCUUCU m8a Disrupted HHHNE_19036_TMEM132B|NM_052907|exon_CDS|-0.919987936338531|-0.371790509209006
hsa-miR-1248 agAAGAAGGgacgag ACCUUCUU m7b (m7b->m6b) HHHNH_3911_TMEM132B|NM_052907|exon_CDS|-1.32186564703218|-0.00528504512946422
hsa-miR-4778-3p aGAAGAAGggacgag UCUUCUUC m7b Disrupted HHHNH_3911_TMEM132B|NM_052907|exon_CDS|-1.32186564703218|-0.00528504512946422
hsa-miR-5088-3p agaAGAAGGGAcgag UCCCUUCU m8a Disrupted HHHNH_3911_TMEM132B|NM_052907|exon_CDS|-1.32186564703218|-0.00528504512946422
hsa-miR-1248 agAAGAAGGgacgag ACCUUCUU m7b (m7b->m6b) HHHSA_6258_TMEM132B|NM_052907|exon_CDS|-0.874998545922905|-0.20274186935389
hsa-miR-4778-3p aGAAGAAGggacgag UCUUCUUC m7b Disrupted HHHSA_6258_TMEM132B|NM_052907|exon_CDS|-0.874998545922905|-0.20274186935389
hsa-miR-5088-3p agaAGAAGGGAcgag UCCCUUCU m8a Disrupted HHHSA_6258_TMEM132B|NM_052907|exon_CDS|-0.874998545922905|-0.20274186935389
hsa-miR-1248 agAAGAAGGgacgag ACCUUCUU m7b (m7b->m6b) HHHSE_19036_TMEM132B|NM_052907|exon_CDS|-0.919987936338531|-0.371790509209006
hsa-miR-4778-3p aGAAGAAGggacgag UCUUCUUC m7b Disrupted HHHSE_19036_TMEM132B|NM_052907|exon_CDS|-0.919987936338531|-0.371790509209006
hsa-miR-5088-3p agaAGAAGGGAcgag UCCCUUCU m8a Disrupted HHHSE_19036_TMEM132B|NM_052907|exon_CDS|-0.919987936338531|-0.371790509209006
hsa-miR-1248 agAAGAAGGgacgag ACCUUCUU m7b (m7b->m6b) HHHSH_3911_TMEM132B|NM_052907|exon_CDS|-1.32186564703218|-0.00528504512946422
hsa-miR-4778-3p aGAAGAAGggacgag UCUUCUUC m7b Disrupted HHHSH_3911_TMEM132B|NM_052907|exon_CDS|-1.32186564703218|-0.00528504512946422
hsa-miR-5088-3p agaAGAAGGGAcgag UCCCUUCU m8a Disrupted HHHSH_3911_TMEM132B|NM_052907|exon_CDS|-1.32186564703218|-0.00528504512946422

Mutation Mutation ID Sample Name Cancer Type
chr12:g.125650708G>T COSM936824 TCGA-B5-A11E-01 [endometrium][NS][carcinoma][endometrioid_carcinoma]
miRNA Targets Table
miR ID miRSite miRSeed SeedClass FuncClass Cluster ID
hsa-miR-4636 tgACGAGTacgatga AACUCGUG m6b Created HHHNA_6258_TMEM132B|NM_052907|exon_CDS|-0.874998545922905|-0.20274186935389
hsa-miR-487b-3p tgacgaGTACGATga AAUCGUAC m7b Created HHHNA_6258_TMEM132B|NM_052907|exon_CDS|-0.874998545922905|-0.20274186935389
hsa-miR-4636 tgACGAGTacgatga AACUCGUG m6b Created HHHNE_19036_TMEM132B|NM_052907|exon_CDS|-0.919987936338531|-0.371790509209006
hsa-miR-487b-3p tgacgaGTACGATga AAUCGUAC m7b Created HHHNE_19036_TMEM132B|NM_052907|exon_CDS|-0.919987936338531|-0.371790509209006
hsa-miR-4636 tgACGAGTacgatga AACUCGUG m6b Created HHHNH_3911_TMEM132B|NM_052907|exon_CDS|-1.32186564703218|-0.00528504512946422
hsa-miR-487b-3p tgacgaGTACGATga AAUCGUAC m7b Created HHHNH_3911_TMEM132B|NM_052907|exon_CDS|-1.32186564703218|-0.00528504512946422
hsa-miR-4636 tgACGAGTacgatga AACUCGUG m6b Created HHHSA_6258_TMEM132B|NM_052907|exon_CDS|-0.874998545922905|-0.20274186935389
hsa-miR-487b-3p tgacgaGTACGATga AAUCGUAC m7b Created HHHSA_6258_TMEM132B|NM_052907|exon_CDS|-0.874998545922905|-0.20274186935389
hsa-miR-4636 tgACGAGTacgatga AACUCGUG m6b Created HHHSE_19036_TMEM132B|NM_052907|exon_CDS|-0.919987936338531|-0.371790509209006
hsa-miR-487b-3p tgacgaGTACGATga AAUCGUAC m7b Created HHHSE_19036_TMEM132B|NM_052907|exon_CDS|-0.919987936338531|-0.371790509209006
hsa-miR-4636 tgACGAGTacgatga AACUCGUG m6b Created HHHSH_3911_TMEM132B|NM_052907|exon_CDS|-1.32186564703218|-0.00528504512946422
hsa-miR-487b-3p tgacgaGTACGATga AAUCGUAC m7b Created HHHSH_3911_TMEM132B|NM_052907|exon_CDS|-1.32186564703218|-0.00528504512946422

Mutation Mutation ID Sample Name Cancer Type
chr12:g.125650704C>A COSM271808 TCGA-AA-3848-01 [large_intestine][colon][carcinoma][adenocarcinoma]
miRNA Targets Table
miR ID miRSite miRSeed SeedClass FuncClass Cluster ID
hsa-miR-1236-3p gcgatGAAGAGGacg CCUCUUCC m7a Created HHHNA_6258_TMEM132B|NM_052907|exon_CDS|-0.874998545922905|-0.20274186935389
hsa-miR-3909 gcgatgaAGAGGACg UGUCCUCU m7b Created HHHNA_6258_TMEM132B|NM_052907|exon_CDS|-0.874998545922905|-0.20274186935389
hsa-miR-6515-3p gcgaTGAAGAGgacg UCUCUUCA m7b Created HHHNA_6258_TMEM132B|NM_052907|exon_CDS|-0.874998545922905|-0.20274186935389
hsa-miR-6852-3p gcgatgaAGAGGACg UGUCCUCU m7b Created HHHNA_6258_TMEM132B|NM_052907|exon_CDS|-0.874998545922905|-0.20274186935389
hsa-miR-6881-3p gcgatgAAGAGGAcg AUCCUCUU m7b Created HHHNA_6258_TMEM132B|NM_052907|exon_CDS|-0.874998545922905|-0.20274186935389
hsa-miR-877-3p gcgatGAAGAGGAcg UCCUCUUC m8a Created HHHNA_6258_TMEM132B|NM_052907|exon_CDS|-0.874998545922905|-0.20274186935389
hsa-miR-1236-3p gcgatGAAGAGGacg CCUCUUCC m7a Created HHHNE_19036_TMEM132B|NM_052907|exon_CDS|-0.919987936338531|-0.371790509209006
hsa-miR-3909 gcgatgaAGAGGACg UGUCCUCU m7b Created HHHNE_19036_TMEM132B|NM_052907|exon_CDS|-0.919987936338531|-0.371790509209006
hsa-miR-6515-3p gcgaTGAAGAGgacg UCUCUUCA m7b Created HHHNE_19036_TMEM132B|NM_052907|exon_CDS|-0.919987936338531|-0.371790509209006
hsa-miR-6852-3p gcgatgaAGAGGACg UGUCCUCU m7b Created HHHNE_19036_TMEM132B|NM_052907|exon_CDS|-0.919987936338531|-0.371790509209006
hsa-miR-6881-3p gcgatgAAGAGGAcg AUCCUCUU m7b Created HHHNE_19036_TMEM132B|NM_052907|exon_CDS|-0.919987936338531|-0.371790509209006
hsa-miR-877-3p gcgatGAAGAGGAcg UCCUCUUC m8a Created HHHNE_19036_TMEM132B|NM_052907|exon_CDS|-0.919987936338531|-0.371790509209006
hsa-miR-1236-3p gcgatGAAGAGGacg CCUCUUCC m7a Created HHHNH_3911_TMEM132B|NM_052907|exon_CDS|-1.32186564703218|-0.00528504512946422
hsa-miR-3909 gcgatgaAGAGGACg UGUCCUCU m7b Created HHHNH_3911_TMEM132B|NM_052907|exon_CDS|-1.32186564703218|-0.00528504512946422
hsa-miR-6515-3p gcgaTGAAGAGgacg UCUCUUCA m7b Created HHHNH_3911_TMEM132B|NM_052907|exon_CDS|-1.32186564703218|-0.00528504512946422
hsa-miR-6852-3p gcgatgaAGAGGACg UGUCCUCU m7b Created HHHNH_3911_TMEM132B|NM_052907|exon_CDS|-1.32186564703218|-0.00528504512946422
hsa-miR-6881-3p gcgatgAAGAGGAcg AUCCUCUU m7b Created HHHNH_3911_TMEM132B|NM_052907|exon_CDS|-1.32186564703218|-0.00528504512946422
hsa-miR-877-3p gcgatGAAGAGGAcg UCCUCUUC m8a Created HHHNH_3911_TMEM132B|NM_052907|exon_CDS|-1.32186564703218|-0.00528504512946422
hsa-miR-1236-3p gcgatGAAGAGGacg CCUCUUCC m7a Created HHHSA_6258_TMEM132B|NM_052907|exon_CDS|-0.874998545922905|-0.20274186935389
hsa-miR-3909 gcgatgaAGAGGACg UGUCCUCU m7b Created HHHSA_6258_TMEM132B|NM_052907|exon_CDS|-0.874998545922905|-0.20274186935389
hsa-miR-6515-3p gcgaTGAAGAGgacg UCUCUUCA m7b Created HHHSA_6258_TMEM132B|NM_052907|exon_CDS|-0.874998545922905|-0.20274186935389
hsa-miR-6852-3p gcgatgaAGAGGACg UGUCCUCU m7b Created HHHSA_6258_TMEM132B|NM_052907|exon_CDS|-0.874998545922905|-0.20274186935389
hsa-miR-6881-3p gcgatgAAGAGGAcg AUCCUCUU m7b Created HHHSA_6258_TMEM132B|NM_052907|exon_CDS|-0.874998545922905|-0.20274186935389
hsa-miR-877-3p gcgatGAAGAGGAcg UCCUCUUC m8a Created HHHSA_6258_TMEM132B|NM_052907|exon_CDS|-0.874998545922905|-0.20274186935389
hsa-miR-1236-3p gcgatGAAGAGGacg CCUCUUCC m7a Created HHHSE_19036_TMEM132B|NM_052907|exon_CDS|-0.919987936338531|-0.371790509209006
hsa-miR-3909 gcgatgaAGAGGACg UGUCCUCU m7b Created HHHSE_19036_TMEM132B|NM_052907|exon_CDS|-0.919987936338531|-0.371790509209006
hsa-miR-6515-3p gcgaTGAAGAGgacg UCUCUUCA m7b Created HHHSE_19036_TMEM132B|NM_052907|exon_CDS|-0.919987936338531|-0.371790509209006
hsa-miR-6852-3p gcgatgaAGAGGACg UGUCCUCU m7b Created HHHSE_19036_TMEM132B|NM_052907|exon_CDS|-0.919987936338531|-0.371790509209006
hsa-miR-6881-3p gcgatgAAGAGGAcg AUCCUCUU m7b Created HHHSE_19036_TMEM132B|NM_052907|exon_CDS|-0.919987936338531|-0.371790509209006
hsa-miR-877-3p gcgatGAAGAGGAcg UCCUCUUC m8a Created HHHSE_19036_TMEM132B|NM_052907|exon_CDS|-0.919987936338531|-0.371790509209006
hsa-miR-1236-3p gcgatGAAGAGGacg CCUCUUCC m7a Created HHHSH_3911_TMEM132B|NM_052907|exon_CDS|-1.32186564703218|-0.00528504512946422
hsa-miR-3909 gcgatgaAGAGGACg UGUCCUCU m7b Created HHHSH_3911_TMEM132B|NM_052907|exon_CDS|-1.32186564703218|-0.00528504512946422
hsa-miR-6515-3p gcgaTGAAGAGgacg UCUCUUCA m7b Created HHHSH_3911_TMEM132B|NM_052907|exon_CDS|-1.32186564703218|-0.00528504512946422
hsa-miR-6852-3p gcgatgaAGAGGACg UGUCCUCU m7b Created HHHSH_3911_TMEM132B|NM_052907|exon_CDS|-1.32186564703218|-0.00528504512946422
hsa-miR-6881-3p gcgatgAAGAGGAcg AUCCUCUU m7b Created HHHSH_3911_TMEM132B|NM_052907|exon_CDS|-1.32186564703218|-0.00528504512946422
hsa-miR-877-3p gcgatGAAGAGGAcg UCCUCUUC m8a Created HHHSH_3911_TMEM132B|NM_052907|exon_CDS|-1.32186564703218|-0.00528504512946422

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