Enhancers that have rs35467460[chr19:2970188]
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Chrom. Start End Enhancer ID Tissues that enhancer appears More
chr19 2960165 2972415 enh17857

Transcript factors that have rs35467460[chr19:2970188]
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Chrom. Start End TF name Source Predicted site? Tissue id More
chr19 2969854 2970905 ZNF274 GTRD no Cervix (HeLa-S3) 21838374
chr19 2969864 2970976 ZNF143 GTRD no Epithelial (MCF-7) 21838375
chr19 2969870 2971005 ZNF143 GTRD no Epithelial (MCF-7) 21838376
chr19 2970007 2970874 ZNF274 GTRD no Cervix (HeLa-S3) 21838377
chr19 2970015 2970481 ZNF143 GTRD no Epithelial (MCF-7) 21838378
chr19 2970038 2970625 ZNF143 GTRD no Epithelial (MCF-7) 21838379
chr19 2970046 2970520 ZNF143 GTRD no Epithelial (MCF-7) 21838380
chr19 2970047 2970780 ZNF143 GTRD no Epithelial (MCF-7) 21838381
chr19 2970085 2970657 ZNF274 GTRD no Cervix (HeLa-S3) 21838382
chr19 2970087 2970636 ZNF143 GTRD no Epithelial (MCF-7) 21838383
chr19 2970093 2970569 ZZZ3 ENCODE Uniform TFBS no Cervix (HeLa-S3) 21838384
chr19 2970105 2970643 ZNF274 GTRD no Cervix (HeLa-S3) 21838385
chr19 2970109 2970535 ZNF143 GTRD no Epithelial (MCF-7) 21838386
chr19 2970109 2970863 ZNF274 GTRD no Cervix (HeLa-S3) 21838387
chr19 2970128 2970733 ZNF274 GTRD no Cervix (HeLa-S3) 21838388
chr19 2970129 2970522 ZNF143 GTRD no Epithelial (MCF-7) 21838389
chr19 2970129 2970803 ZNF143 GTRD no Epithelial (MCF-7) 21838390
chr19 2970132 2970443 ZNF143 GTRD no Epithelial (MCF-7) 21838391
chr19 2970138 2970723 ZNF274 GTRD no Cervix (HeLa-S3) 21838392
chr19 2970142 2970472 ZZZ3 ENCODE Uniform TFBS no Cervix (HeLa-S3) 21838393
chr19 2970165 2970500 ZNF143 GTRD no Epithelial (MCF-7) 21838394
chr19 2970179 2970191 MEF2D JASPAR yes 112105362
chr19 2970181 2970196 FOXP1 JASPAR yes 112105363
chr19 2970182 2970198 POU4F2 JASPAR yes 112105364
chr19 2970183 2970199 POU4F3 JASPAR yes 112105365
chr19 2970185 2970199 POU4F1 JASPAR yes 112105366
chr19 2970185 2970200 HNF1A JASPAR yes 112105367
chr19 2970185 2970206 IRF1 JASPAR yes 112105368
chr19 2970187 2970193 TBP TRANSFAC yes 112105369

Genes associated with rs35467460[chr19:2970188], 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