Tag | Content |
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EnhancerAtlas ID | HS091-39744 |
Organism | Homo sapiens |
Tissue/cell | HepG2 |
Coordinate | chr5:176516700-176517390 |
Target genes | Number: 12 | Name | Ensembl ID |
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SNPs | Number: 1 | ID | Chromosome | Position | Genome Version |
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TF binding sites/motifs | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
NR2C2 | MA0504.1 | chr5:176517367-176517382 | TGACCTCTGCCCTCT | - | 7.31 |
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| Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder | Number of disease enhancers: 2 | Chromosome | Start | End |
chr5 | 176517155 | 176517301 | chr5 | 176516802 | 176517081 |
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Enhancer Sequence | CTTCTGAGGT GGGAGAGGGT GGCAGGGGTG GGAAGAGTGG GCACCAGGAG GGGGCTGCTG 60 GGCTGAGCAA AGCTGGAAAG GATCCTTGCC CAGGCCCTGA GAAGGTGGCG GCAGGGCAGG 120 GCTCAACCAC TGAGACTCAG TCAGTGCCTG GCTTCCAGCA AGCATTCATC TATCACTGTG 180 TCTGCGAGAG AGGACTGGCC TTGCAGGGCG CAGGGCCCTA AGCTGGGCTG CAGAGCTGGT 240 GGTGAGCTCC TTACCTGGGT GTGTGTGCGT GTGTGTGTGT GTTCTGTGCA CTGGGTGTGT 300 GACCTAGGAG GTCCAGGCAG CATGTGTGGT ATAAGCATTA TGAGGGTGAT ATGCCCCGGT 360 GCAGCATGAC CCTGTATGTG GCACCAACAG CATGTGCCTT GTGTGTGTGT GTGTCCGTAT 420 GTGTGTGTGT GTATGCGTGT GTGTGTGTGT GTGTGTCTTG GCCACTGTCG TGTGCACTAA 480 ATGCTGTGTG TGTGACATGC CCCAAGAGTG TGGCATTTGC CCTGGGTGTG GCATCCGCAG 540 CATGTGGCTG TGTGGGTGTC AAGGAGTGGT GGCTCCTTCA GCATGCGTTG CAAAGTGCTT 600 GTGCCCTGCA TGTGCGGTGT GTTCTTTGTA CACAGGAGGC TGCCTCAGAT GGGGCTGCGG 660 GGTCTGCTGA CCTCTGCCCT CTGCCCACAG 690
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