Enhancers that regulate NR2C1[ENSG00000120798.12]
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Chrom. Start End Enhancer ID TSS of gene Distance between enhancer and TSS Tissues that enhancer appears More
chr12 95372465 95386255 enh2524 95467479 81224
chr12 95404686 95404921 vista14529 95467479 62558
chr12 95411707 95411975 vista14530 95467479 55504
chr12 95477787 95477978 vista14531 95467479 10308
chr12 95488285 95497975 enh14915 95467479 20806
chr12 95492031 95492186 vista14532 95467479 24552
chr12 95507591 95515363 enh86139 95467479 40112
chr12 95508307 95508578 vista14533 95467479 40828
chr12 95523765 95527995 enh14916 95467479 56286
chr12 95534293 95541455 enh64621 95467479 66814
chr12 95555365 95565496 enh29883 95467479 87886

Transcript facotrs that regulate NR2C1[ENSG00000120798.12]
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Chrom. Start End TF name Source Predicted site? Tissue TSS of gene Distance between TFBS and gene id More

Chrom. Position dbSNP ID Reference Allele Alternative Allele Distance between TSS and SNP Tissue q Value id More
chr12 95158731 rs142807680 G GC 255274 Heart 0.100272 2822184
chr12 96088828 rs4762601 T C 621349 Pancreas 0.140864 2828912
chr12 95535987 rs77475611 G A 68508 Spleen 0.301546 2824323
chr12 96167151 rs12298589 G T 699672 Ovary 0.250986 2829658
chr12 94662513 rs112647419 G C,T 751492 Liver 0.274736 2818981
chr12 95570846 rs7310428 T G 103367 Lung 0.0244235 2824536

Genomic Location chr12:95414005-95467479[-]
TSS 95467479
Gene Name NR2C1
Ensembl ID ENSG00000120798.12
ENTREZID 7181
Uniprot
H9NIM2
P13056
H9NIM3
Protein Name
group C
group C isoform
isoform CRA_c
member 1
Nuclear receptor subfamily 2
Nuclear receptor subfamily 2
Nuclear receptor subfamily 2 group C member 1