Enhancers that have rs4899551[chr14:75660246]
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Chrom. Start End Enhancer ID Tissues that enhancer appears More

Transcript factors that have rs4899551[chr14:75660246]
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Chrom. Start End TF name Source Predicted site? Tissue id More
chr14 75659834 75661941 ZNF274 GTRD no Blood (GM12878) 21629480
chr14 75659850 75662114 ZNF274 GTRD no Cervix (HeLa-S3) 21629481
chr14 75659850 75662114 ZNF274 GTRD no Cervix (HeLa-S3) 21629482
chr14 75659880 75662026 ZNF274 GTRD no Liver (HepG2) 21629483
chr14 75659881 75662548 ZNF143 GTRD no Epithelial (MCF-7) 21629484
chr14 75660001 75661924 ZNF274 GTRD no Blood (GM12878) 21629485
chr14 75660028 75661634 ZNF274 GTRD no Blood (GM12878) 21629486
chr14 75660041 75661954 ZNF274 GTRD no Liver (HepG2) 21629487
chr14 75660104 75661710 ZNF274 GTRD no Cervix (HeLa-S3) 21629488
chr14 75660132 75661834 ZNF274 GTRD no Liver (HepG2) 21629489
chr14 75660214 75662348 ZNF143 GTRD no Epithelial (MCF-7) 21629490
chr14 75660221 75662146 ZNF143 GTRD no Epithelial (MCF-7) 21629491

Genes associated with rs4899551[chr14:75660246], 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
chr14 75408537 75422487 - PGF ENSG00000119630.9 75422487 237759 Esophagus 0.019543 13488