Enhancers that have rs34751799[chr14:65192877]
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Chrom. Start End Enhancer ID Tissues that enhancer appears More
chr14 65180405 65194302 enh15685
chr14 65192675 65192925 vista18108

Transcript factors that have rs34751799[chr14:65192877]
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Chrom. Start End TF name Source Predicted site? Tissue id More
chr14 65192481 65193019 SOX2 GTRD no Neural Stem Cells (H9) 21623168
chr14 65192481 65193019 SOX2 GTRD no Neural Stem Cells (H9) 108107279
chr14 65192538 65193100 SOX2 GTRD no Neural Stem Cells (H9) 21623169
chr14 65192538 65193100 SOX2 GTRD no Neural Stem Cells (H9) 108107280
chr14 65192631 65192991 SOX2 GTRD no Neural Stem Cells (H9) 21623170
chr14 65192631 65192991 SOX2 GTRD no Neural Stem Cells (H9) 108107281
chr14 65192639 65193027 SOX2 GTRD no Neural Stem Cells (H9) 21623171
chr14 65192639 65193027 SOX2 GTRD no Neural Stem Cells (H9) 108107282
chr14 65192646 65193198 ZNF274 GTRD no Bone Marrow (K562) 108107283
chr14 65192669 65192939 ZNF143 ENCODE Uniform TFBS no Embryonic Stem Cell Line (H1-hESC) 108107284
chr14 65192671 65192961 ZBTB33 ENCODE Uniform TFBS no Colon (HCT116) 108107285
chr14 65192783 65193034 ZNF274 GTRD no Bone Marrow (K562) 108107286
chr14 65192870 65192878 GATA5 JASPAR yes 107565036
chr14 65192870 65192878 GATA5 JASPAR yes 116015104

Genes associated with rs34751799[chr14:65192877], 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