Enhancers that have rs200999928[chr7:130068763]
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Chrom. Start End Enhancer ID Tissues that enhancer appears More
chr7 130067882 130075575 enh24513

Transcript factors that have rs200999928[chr7:130068763]
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Chrom. Start End TF name Source Predicted site? Tissue id More
chr7 130068752 130068766 ONECUT2 JASPAR yes 18015726
chr7 130068752 130068766 ONECUT3 JASPAR yes 18015727
chr7 130068752 130068767 FOXP1 JASPAR yes 18015728
chr7 130068753 130068768 FOXA1 JASPAR yes 18015729
chr7 130068754 130068765 FOXB1 JASPAR yes 18015730
chr7 130068754 130068765 FOXC1 JASPAR yes 18015731
chr7 130068754 130068766 FOXC2 JASPAR yes 18015732
chr7 130068755 130068767 FOXI1 JASPAR yes 18015733
chr7 130068756 130068770 ONECUT2 JASPAR yes 18015734
chr7 130068756 130068770 ONECUT3 JASPAR yes 18015735
chr7 130068756 130068771 FOXP1 JASPAR yes 18015736
chr7 130068756 130068771 HNF1A JASPAR yes 18015737
chr7 130068757 130068771 POU4F1 JASPAR yes 18015738
chr7 130068757 130068772 FOXA1 JASPAR yes 18015739
chr7 130068757 130068773 POU4F2 JASPAR yes 18015740
chr7 130068757 130068773 POU4F3 JASPAR yes 18015741
chr7 130068758 130068769 FOXB1 JASPAR yes 18015742
chr7 130068758 130068769 FOXC1 JASPAR yes 18015743
chr7 130068758 130068769 PROP1 JASPAR yes 18015744
chr7 130068758 130068770 FOXC2 JASPAR yes 18015745
chr7 130068759 130068771 FOXI1 JASPAR yes 18015746
chr7 130068760 130068774 ONECUT2 JASPAR yes 18015747
chr7 130068760 130068774 ONECUT3 JASPAR yes 18015748
chr7 130068760 130068775 FOXP1 JASPAR yes 18015749
chr7 130068760 130068775 HNF1A JASPAR yes 18015750
chr7 130068761 130068775 POU4F1 JASPAR yes 18015751
chr7 130068761 130068776 FOXA1 JASPAR yes 18015752
chr7 130068761 130068777 POU4F2 JASPAR yes 18015753
chr7 130068761 130068777 POU4F3 JASPAR yes 18015754
chr7 130068762 130068773 FOXB1 JASPAR yes 18015755
chr7 130068762 130068773 FOXC1 JASPAR yes 18015756
chr7 130068762 130068773 PROP1 JASPAR yes 18015757
chr7 130068762 130068774 FOXC2 JASPAR yes 18015758
chr7 130068763 130068775 FOXI1 JASPAR yes 18015759

Genes associated with rs200999928[chr7:130068763], 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