Enhancers that have rs17099812[chr14:74868828]
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Chrom. Start End Enhancer ID Tissues that enhancer appears More
chr14 74865125 74871695 enh3323
chr14 74868763 74868996 vista18434

Transcript factors that have rs17099812[chr14:74868828]
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Chrom. Start End TF name Source Predicted site? Tissue id More
chr14 74868235 74868895 ZZZ3 ENCODE Uniform TFBS no Blood (GM12878) 108113151
chr14 74868235 74868895 ZZZ3 ENCODE Uniform TFBS no Blood (GM12878) 108113152
chr14 74868623 74869143 ZNF143 ENCODE Uniform TFBS no Embryonic Stem Cell Line (H1-hESC) 108113153
chr14 74868634 74868944 ZZZ3 ENCODE Uniform TFBS no Blood (GM12878) 108113154
chr14 74868701 74869025 ZNF143 ENCODE Uniform TFBS no Embryonic Stem Cell Line (H1-hESC) 108113155
chr14 74868741 74868985 ZNF143 ENCODE Uniform TFBS no Embryonic Stem Cell Line (H1-hESC) 108113157
chr14 74868748 74868870 ZZZ3 ENCODE Uniform TFBS no Blood (GM12878) 108113158
chr14 74868812 74868831 PAX5 JASPAR yes 107581112
chr14 74868812 74868831 PAX5 JASPAR yes 116564428
chr14 74868813 74868828 ESR2 JASPAR yes 107581113
chr14 74868813 74868828 ESR2 JASPAR yes 116564429
chr14 74868815 74868832 PAX1 JASPAR yes 107581115
chr14 74868815 74868832 PAX9 JASPAR yes 107581116
chr14 74868815 74868832 PAX1 JASPAR yes 116564431
chr14 74868815 74868832 PAX9 JASPAR yes 116564432

Genes associated with rs17099812[chr14:74868828], 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