EnhancerDB
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  3. rs192327611[chr19:1172032]
Enhancers that have rs192327611[chr19:1172032]
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Chrom. Start End Enhancer ID Tissues that enhancer appears More
chr19 1159608 1173238 enh17838
Bone Marrow (K562) Cervix (HeLa-S3) Prostate (RWPE1) Esophagus Bone (Osteoblast) Placenta Thyroid Uterus Stomach
chr19 1171933 1172315 vista28144
VISTA
Transcript factors that have rs192327611[chr19:1172032]
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Chrom. Start End TF name Source Predicted site? Tissue id More
chr19 1167320 1174938 ZNF274 GTRD no Cervix (HeLa-S3) 21831465
chr19 1167320 1174938 ZNF274 GTRD no Cervix (HeLa-S3) 108350492
chr19 1167320 1174938 ZNF274 GTRD no Cervix (HeLa-S3) 108350493
chr19 1167320 1174938 ZNF274 GTRD no Cervix (HeLa-S3) 108350494
chr19 1167320 1174938 ZNF274 GTRD no Cervix (HeLa-S3) 108350495
chr19 1168874 1172383 ZNF143 GTRD no Epithelial (MCF-7) 108350530
chr19 1168874 1172383 ZNF143 GTRD no Epithelial (MCF-7) 108350531
chr19 1168874 1172383 ZNF143 GTRD no Epithelial (MCF-7) 108350532
chr19 1169856 1172226 ZNF143 GTRD no Epithelial (MCF-7) 108350606
chr19 1169856 1172226 ZNF143 GTRD no Epithelial (MCF-7) 108350607
chr19 1169856 1172226 ZNF143 GTRD no Epithelial (MCF-7) 108350608
chr19 1171074 1172157 ZNF143 GTRD no Epithelial (MCF-7) 108350688
chr19 1171074 1172157 ZNF143 GTRD no Epithelial (MCF-7) 108350689
chr19 1171118 1174983 TCF7L2 GTRD no Colon (HCT116) 108350692
chr19 1171118 1174983 TCF7L2 GTRD no Colon (HCT116) 108350693
chr19 1171118 1174983 TCF7L2 GTRD no Colon (HCT116) 108350694
chr19 1171244 1174775 ZNF274 GTRD no Bone Marrow (K562) 21831541
chr19 1171244 1174775 ZNF274 GTRD no Bone Marrow (K562) 108350698
chr19 1171244 1174775 ZNF274 GTRD no Bone Marrow (K562) 108350699
chr19 1171250 1174550 ZNF143 GTRD no Epithelial (MCF-7) 21831542
chr19 1171250 1174550 ZNF143 GTRD no Epithelial (MCF-7) 108350700
chr19 1171250 1174550 ZNF143 GTRD no Epithelial (MCF-7) 108350701
chr19 1171252 1174691 TCF7L2 GTRD no Colon (HCT116) 108350702
chr19 1171252 1174691 TCF7L2 GTRD no Colon (HCT116) 108350703
chr19 1171279 1172125 TCF7L2 GTRD no Colon (HCT116) 108350704
chr19 1171345 1172476 ZNF143 GTRD no Epithelial (MCF-7) 108350706
chr19 1171384 1175424 TCF7L2 GTRD no Colon (HCT116) 108350707
chr19 1171384 1175424 TCF7L2 GTRD no Colon (HCT116) 108350708
chr19 1171427 1174756 TCF7L2 GTRD no Colon (HCT116) 108350709
chr19 1171427 1174756 TCF7L2 GTRD no Colon (HCT116) 108350710
chr19 1171630 1172035 ZNF274 GTRD no Liver (HepG2) 108350711
chr19 1171702 1174970 ZNF274 GTRD no Cervix (HeLa-S3) 21831543
chr19 1171702 1174970 ZNF274 GTRD no Cervix (HeLa-S3) 108350713
chr19 1171702 1174970 ZNF274 GTRD no Cervix (HeLa-S3) 108350714
chr19 1171710 1172899 TCF7L2 GTRD no Colon (HCT116) 108350715
chr19 1171710 1172899 TCF7L2 GTRD no Colon (HCT116) 108350716
chr19 1171744 1173709 ZBTB33 GTRD no Lung (A549) 108350717
chr19 1171744 1173709 ZBTB33 GTRD no Lung (A549) 108350718
chr19 1171751 1172170 ZNF274 GTRD no Blood (GM12878) 108350719
chr19 1171757 1173371 ZNF143 GTRD no Epithelial (MCF-7) 108350720
chr19 1171757 1173371 ZNF143 GTRD no Epithelial (MCF-7) 108350721
chr19 1171768 1174972 ZNF274 GTRD no Blood (GM12878) 108350722
chr19 1171768 1174972 ZNF274 GTRD no Blood (GM12878) 108350723
chr19 1171770 1172403 ZNF274 GTRD no Bone Marrow (K562) 21831544
chr19 1171770 1172403 ZNF274 GTRD no Bone Marrow (K562) 108350724
chr19 1171840 1174880 TCF7L2 GTRD no Colon (HCT116) 108350725
chr19 1171840 1174880 TCF7L2 GTRD no Colon (HCT116) 108350726
chr19 1171845 1172045 ZNF274 ENCODE Uniform TFBS no Bone Marrow (K562) 21831545
chr19 1171845 1172045 ZNF274 ENCODE Uniform TFBS no Bone Marrow (K562) 108350727
chr19 1171981 1174051 ZBTB33 GTRD no Lung (A549) 108350728
chr19 1171981 1174051 ZBTB33 GTRD no Lung (A549) 108350729
chr19 1171988 1172775 ZBTB33 GTRD no Lung (A549) 108350730
chr19 1172021 1172461 TCF7L2 ENCODE Uniform TFBS no Pancreas (Panc1) 108350731
chr19 1172022 1172033 E2F6 JASPAR yes 70779196
chr19 1172022 1172033 E2F6 JASPAR yes 111997952
chr19 1172025 1172035 SP1 JASPAR yes 70779197
chr19 1172025 1172035 SP1 JASPAR yes 111997953
Genes associated with rs192327611[chr19:1172032], 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