Enhancers that have rs376612956[chr14:71766170]
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Chrom. Start End Enhancer ID Tissues that enhancer appears More
chr14 71765225 71769375 enh112346

Transcript factors that have rs376612956[chr14:71766170]
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Chrom. Start End TF name Source Predicted site? Tissue id More
chr14 71766165 71766175 EN2 JASPAR yes 116408869
chr14 71766165 71766175 ESX1 JASPAR yes 116408870
chr14 71766165 71766175 GBX1 JASPAR yes 116408871
chr14 71766165 71766175 GBX2 JASPAR yes 116408872
chr14 71766165 71766175 GSX2 JASPAR yes 116408873
chr14 71766165 71766175 HESX1 JASPAR yes 116408874
chr14 71766165 71766175 LBX2 JASPAR yes 116408875
chr14 71766165 71766175 LHX2 JASPAR yes 116408876
chr14 71766165 71766175 MIXL1 JASPAR yes 116408877
chr14 71766165 71766175 RAX JASPAR yes 116408878
chr14 71766166 71766174 BARX1 JASPAR yes 116408879
chr14 71766166 71766174 BSX JASPAR yes 116408880
chr14 71766166 71766174 EN1 JASPAR yes 116408881
chr14 71766166 71766174 ISX JASPAR yes 116408882
chr14 71766166 71766174 LHX9 JASPAR yes 116408883
chr14 71766166 71766174 MSX1 JASPAR yes 116408884
chr14 71766166 71766174 MSX2 JASPAR yes 116408885
chr14 71766166 71766174 PRRX1 JASPAR yes 116408886
chr14 71766166 71766174 RAX2 JASPAR yes 116408887
chr14 71766166 71766174 SHOX JASPAR yes 116408888
chr14 71766168 71766178 NFIA JASPAR yes 116408889
chr14 71766170 71766176 NFIC JASPAR yes 116408890

Genes associated with rs376612956[chr14:71766170], 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