| Tag | Content |
|---|
EnhancerAtlas ID | HS183-06858 | Organism | Homo sapiens | Tissue/cell | T47D-MTVL | Coordinate | chr5:176516690-176517390 | SNPs | | Number: 1 | ID | Chromosome | Position | Genome Version |
| TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| NR2C2 | MA0504.1 | chr5:176517367-176517382 | TGACCTCTGCCCTCT | - | 7.31 |
| | | 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 |
| Enhancer Sequence | CTTGGTATGG CTTCTGAGGT GGGAGAGGGT GGCAGGGGTG GGAAGAGTGG GCACCAGGAG 60
GGGGCTGCTG GGCTGAGCAA AGCTGGAAAG GATCCTTGCC CAGGCCCTGA GAAGGTGGCG 120
GCAGGGCAGG GCTCAACCAC TGAGACTCAG TCAGTGCCTG GCTTCCAGCA AGCATTCATC 180
TATCACTGTG TCTGCGAGAG AGGACTGGCC TTGCAGGGCG CAGGGCCCTA AGCTGGGCTG 240
CAGAGCTGGT GGTGAGCTCC TTACCTGGGT GTGTGTGCGT GTGTGTGTGT GTTCTGTGCA 300
CTGGGTGTGT GACCTAGGAG GTCCAGGCAG CATGTGTGGT ATAAGCATTA TGAGGGTGAT 360
ATGCCCCGGT GCAGCATGAC CCTGTATGTG GCACCAACAG CATGTGCCTT GTGTGTGTGT 420
GTGTCCGTAT GTGTGTGTGT GTATGCGTGT GTGTGTGTGT GTGTGTCTTG GCCACTGTCG 480
TGTGCACTAA ATGCTGTGTG TGTGACATGC CCCAAGAGTG TGGCATTTGC CCTGGGTGTG 540
GCATCCGCAG CATGTGGCTG TGTGGGTGTC AAGGAGTGGT GGCTCCTTCA GCATGCGTTG 600
CAAAGTGCTT GTGCCCTGCA TGTGCGGTGT GTTCTTTGTA CACAGGAGGC TGCCTCAGAT 660
GGGGCTGCGG GGTCTGCTGA CCTCTGCCCT CTGCCCACAG 700
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