Tag | Content |
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EnhancerAtlas ID | HS080-02872 | Organism | Homo sapiens | Tissue/cell | H9 | Coordinate | chr1:204119280-204120720 | TF binding sites/motifs | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
NR3C2 | MA0727.1 | chr1:204119480-204119497 | CAGAACACTATGTCCTG | - | 6.04 | NR3C2 | MA0727.1 | chr1:204119480-204119497 | CAGAACACTATGTCCTG | + | 6.09 |
| | Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder | Number of disease enhancers: 1 | Chromosome | Start | End |
| Enhancer Sequence | ATAGAGTTCA AGAAAAAAAT GGTAGCTTGG GTTTAGCTCC CACACACTCC TGGGTGTGCC 60 TCTAGTGAAT GGGATTTGGC AGTGGAGAAA TTTCCACACT ACTTGGGAGG TAGACGCCTC 120 CTGCTGCTCC TTACCCTCCA CCCCAGTACG GAAAGAAACA TCATGGACCA GAATGTGGCA 180 GGGGAGGGCT GGGAGTTGCC CAGAACACTA TGTCCTGACC AGCTGCCAAT CACCTTGTGC 240 CGGGCAGTGT GCTCTGCTCT ACCCCTTGCC CCATCCAGTG GTGGAGGTAC AAGGAGGGTA 300 CTGAGGTTGG CACCCATCCC AGGACTTTAG TGGCCAGAGG TCCTTACCAG AAAAGACAGG 360 AGACAACTGG GCTGCGAGCA AGGTTCTCTG GACAGCAGGG TGATGAGGAG AAAGGAACCA 420 TGGAATTTAC GGGGCACAAT GTGACAGAGC TGGGAGGGCC CTAGAGGTCA TCTGAACCAA 480 TTCTACGTAG GGAAACTGAG GCAGGAGAGG GGAGGGACTG GCAGATAGCA CGTTAGATCA 540 GTGCTGGAAT TAACCTCAGG CCTGCTTGAT GCCTTGACAG TCTTATACCA AACTGGGCCT 600 TTTATTTTGA AAACGCTACT CCATCCCCAG GGCGGGTTCT GTCAGCCTCC ACACTTGGTT 660 AAGAACCTCC CCACAACTTT GCCCCCACCC CACCCCAGAA TGCCTGTCTG CATGGAGCCG 720 CTACCATTCC AGCACAAGCT ACAAGCGCCC CACTCGGCAC CTTCCTCCAC AGGCAGCCCA 780 CAGCGGGGCT GGAGGTAGTC AGCTGGGGAG TTAGCCTAAG GCTCAGTGAG TGGCTCTGCC 840 CACAGGTGTG TCCTGGGACC TGTGTCCAGC TGGGGCTGGG GAAGATGGCC TGTGTGGGGG 900 TGCTGAGCCC GAGCCTGCAG CGATGGTGAG GAGCTGAGTG CTAGCTGGAA TTCCACAGGG 960 TGGCTCCTGG GACCCACAGG GGCAGCTCAG AGCCTGGAGG ATTTGCTCCC ACCATGGGGT 1020 GGAGAAGGGG CAGCAATGTA TGCATGTATG GCTGGGTCGG GGGGGCGGGG GGTCTCTTAA 1080 AAGTTCCCGC CTCCTCAGGT TTCAGAGCTG GCTGGGTACG CGCTTCTGGT CAGCGAGGGG 1140 CACCAGCACG CAGCGACAGG GGGTGCGGCC CGCACACGCA GCATGCCGAC AGTGGGCAGG 1200 TGGCCACCAG GCGTGCCTAA GAGCCCCGGG AGGAGGGGGG CGTGTGCAGG GCCAAGGGAG 1260 GTGTGAGCCT AGTTTTGGTA GCGACGAAAT CAATCCGTAC ACAAACCACG TTCCAAACCT 1320 TTCTTGCGCA GCAGCCGCGC ACCCCTGGGA CTGACACCCG GAAGGATGCG AGGACTGGGT 1380 CCCCGCATCC CCCTGGCAGC CCTGGCAGGA CCCCATCCTC GGCCCCGCGC CCACTCCGCT 1440
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