Enhancers that have rs34507882[chr17:5000988]
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Chrom. Start End Enhancer ID Tissues that enhancer appears More
chr17 5000892 5001205 vista23816

Transcript factors that have rs34507882[chr17:5000988]
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Chrom. Start End TF name Source Predicted site? Tissue id More
chr17 5000024 5001026 TEF1 GTRD no Bone (Osteoblast) 108233081
chr17 5000529 5001129 ZNF143 ENCODE Uniform TFBS no Embryonic Stem Cell Line (H1-hESC) 108233082
chr17 5000759 5001135 ZNF143 ENCODE Uniform TFBS no Embryonic Stem Cell Line (H1-hESC) 108233083
chr17 5000786 5001142 ZNF143 ENCODE Uniform TFBS no Embryonic Stem Cell Line (H1-hESC) 108233084
chr17 5000803 5001092 ZNF143 ENCODE Uniform TFBS no Embryonic Stem Cell Line (H1-hESC) 108233085
chr17 5000810 5001140 ZNF143 ENCODE Uniform TFBS no Embryonic Stem Cell Line (H1-hESC) 108233086
chr17 5000819 5001109 ZNF143 ENCODE Uniform TFBS no Embryonic Stem Cell Line (H1-hESC) 108233087
chr17 5000850 5001126 ZNF143 ENCODE Uniform TFBS no Embryonic Stem Cell Line (H1-hESC) 108233088
chr17 5000853 5001093 SP2 UCSC Txn Factor no Conserved 108233089
chr17 5000853 5001093 ZNF143 ENCODE Uniform TFBS no Embryonic Stem Cell Line (H1-hESC) 108233090
chr17 5000894 5001674 ZNF143 GTRD no Epithelial (MCF-7) 108233091

Genes associated with rs34507882[chr17:5000988], 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