EnhancerDB
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  3. rs312787[chr11:68120665]
Enhancers that have rs312787[chr11:68120665]
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Chrom. Start End Enhancer ID Tissues that enhancer appears More
chr11 68117352 68125035 enh14025
Skin (Keratinocyte) Prostate (PC-3) Cervix (HeLa-S3) Epithelial (MCF-7) Brain (SK-N-SH) Prostate (RWPE1) Lung (PC-9) Esophagus Astrocyte Bone (Osteoblast) Stomach Muscle (A673) Placenta Colon (HCT116) Breast Thyroid Muscle (Myoblast) Pancreas Uterus Heart
Transcript factors that have rs312787[chr11:68120665]
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Chrom. Start End TF name Source Predicted site? Tissue id More
chr11 68118268 68122643 ZNF274 GTRD no Blood (GM12878) 107984464
chr11 68119723 68122594 ZNF274 GTRD no Liver (HepG2) 107984465
chr11 68119833 68122665 ZNF274 GTRD no Blood (GM12878) 107984466
chr11 68119939 68122497 ZNF274 GTRD no Bone Marrow (K562) 107984467
chr11 68120133 68122061 ZNF274 GTRD no Blood (GM12878) 107984468
chr11 68120233 68122595 ZNF274 GTRD no Cervix (HeLa-S3) 21498245
chr11 68120233 68122595 ZNF274 GTRD no Cervix (HeLa-S3) 107984469
chr11 68120254 68121933 ZNF274 GTRD no Blood (GM12878) 107984470
chr11 68120273 68122393 ZNF274 GTRD no Blood (GM12878) 107984471
chr11 68120276 68122594 ZNF274 GTRD no Liver (HepG2) 107984472
chr11 68120292 68122600 ZNF274 GTRD no Liver (HepG2) 107984473
chr11 68120307 68122489 TCF7L2 GTRD no Colon (HCT116) 21498246
chr11 68120307 68122489 TCF7L2 GTRD no Colon (HCT116) 107984474
chr11 68120311 68122530 ZNF274 GTRD no Bone Marrow (K562) 107984475
chr11 68120336 68122655 ZNF274 GTRD no Liver (HepG2) 107984476
chr11 68120351 68122412 TCF7L2 GTRD no Colon (HCT116) 21498247
chr11 68120351 68122412 TCF7L2 GTRD no Colon (HCT116) 107984477
chr11 68120373 68122427 ZNF274 GTRD no Bone Marrow (K562) 107984478
chr11 68120406 68122581 ZNF274 GTRD no Liver (HepG2) 107984479
chr11 68120430 68122480 TCF7L2 GTRD no Colon (HCT116) 21498248
chr11 68120430 68122480 TCF7L2 GTRD no Colon (HCT116) 107984480
chr11 68120431 68122618 TCF7L2 GTRD no Colon (HCT116) 21498249
chr11 68120431 68122618 TCF7L2 GTRD no Colon (HCT116) 107984481
chr11 68120439 68122411 TCF7L2 GTRD no Colon (HCT116) 21498250
chr11 68120439 68122411 TCF7L2 GTRD no Colon (HCT116) 107984482
chr11 68120445 68122529 ZNF143 GTRD no Epithelial (MCF-7) 21498251
chr11 68120445 68122529 ZNF143 GTRD no Epithelial (MCF-7) 107984483
chr11 68120451 68122550 ZNF274 GTRD no Liver (HepG2) 107984484
chr11 68120479 68122421 ZNF143 GTRD no Epithelial (MCF-7) 21498252
chr11 68120479 68122421 ZNF143 GTRD no Epithelial (MCF-7) 107984485
chr11 68120497 68122012 TCF7L2 GTRD no Colon (HCT116) 21498253
chr11 68120497 68122012 TCF7L2 GTRD no Colon (HCT116) 107984486
chr11 68120501 68121881 TCF7L2 GTRD no Colon (HCT116) 21498254
chr11 68120501 68121881 TCF7L2 GTRD no Colon (HCT116) 107984487
chr11 68120532 68122447 TCF7L2 GTRD no Colon (HCT116) 21498255
chr11 68120532 68122447 TCF7L2 GTRD no Colon (HCT116) 107984488
chr11 68120533 68122696 TCF7L2 GTRD no Colon (HCT116) 21498256
chr11 68120533 68122696 TCF7L2 GTRD no Colon (HCT116) 107984489
chr11 68120545 68122589 ZNF143 GTRD no Epithelial (MCF-7) 21498257
chr11 68120545 68122589 ZNF143 GTRD no Epithelial (MCF-7) 107984490
chr11 68120552 68122524 ZNF274 GTRD no Bone Marrow (K562) 107984491
chr11 68120553 68122551 TCF7L2 GTRD no Colon (HCT116) 21498258
chr11 68120553 68122551 TCF7L2 GTRD no Colon (HCT116) 107984492
chr11 68120572 68122463 ZNF274 GTRD no Cervix (HeLa-S3) 21498259
chr11 68120572 68122463 ZNF274 GTRD no Cervix (HeLa-S3) 107984493
chr11 68120582 68122173 TCF7L2 GTRD no Colon (HCT116) 21498260
chr11 68120582 68122173 TCF7L2 GTRD no Colon (HCT116) 107984494
chr11 68120586 68122286 ZNF274 GTRD no Bone Marrow (K562) 107984495
chr11 68120591 68122431 ZNF274 GTRD no Bone Marrow (K562) 107984496
chr11 68120599 68122551 ZNF143 GTRD no Epithelial (MCF-7) 21498261
chr11 68120599 68122551 ZNF143 GTRD no Epithelial (MCF-7) 107984497
chr11 68120629 68121807 TCF7L2 GTRD no Colon (HCT116) 21498262
chr11 68120629 68121807 TCF7L2 GTRD no Colon (HCT116) 107984498
chr11 68120656 68120670 PLAG1 JASPAR yes 39465652
Genes associated with rs312787[chr11:68120665], comfirmed by eQTL
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Blank TSI value indicates lack of sufficient expression for calculation
Chrom. Start End Strand Gene name Ensembl ID TSS of gene Distance between TSS and SNP Tissue q Value id More