Tag | Content |
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EnhancerAtlas ID | HS092-04410 |
Organism | Homo sapiens |
Tissue/cell | HFF |
Coordinate | chr1:204119290-204120720 |
Target genes | |
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 |
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| Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder | Number of disease enhancers: 1 | Chromosome | Start | End |
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Enhancer Sequence | AGAAAAAAAT GGTAGCTTGG GTTTAGCTCC CACACACTCC TGGGTGTGCC TCTAGTGAAT 60 GGGATTTGGC AGTGGAGAAA TTTCCACACT ACTTGGGAGG TAGACGCCTC CTGCTGCTCC 120 TTACCCTCCA CCCCAGTACG GAAAGAAACA TCATGGACCA GAATGTGGCA GGGGAGGGCT 180 GGGAGTTGCC CAGAACACTA TGTCCTGACC AGCTGCCAAT CACCTTGTGC CGGGCAGTGT 240 GCTCTGCTCT ACCCCTTGCC CCATCCAGTG GTGGAGGTAC AAGGAGGGTA CTGAGGTTGG 300 CACCCATCCC AGGACTTTAG TGGCCAGAGG TCCTTACCAG AAAAGACAGG AGACAACTGG 360 GCTGCGAGCA AGGTTCTCTG GACAGCAGGG TGATGAGGAG AAAGGAACCA TGGAATTTAC 420 GGGGCACAAT GTGACAGAGC TGGGAGGGCC CTAGAGGTCA TCTGAACCAA TTCTACGTAG 480 GGAAACTGAG GCAGGAGAGG GGAGGGACTG GCAGATAGCA CGTTAGATCA GTGCTGGAAT 540 TAACCTCAGG CCTGCTTGAT GCCTTGACAG TCTTATACCA AACTGGGCCT TTTATTTTGA 600 AAACGCTACT CCATCCCCAG GGCGGGTTCT GTCAGCCTCC ACACTTGGTT AAGAACCTCC 660 CCACAACTTT GCCCCCACCC CACCCCAGAA TGCCTGTCTG CATGGAGCCG CTACCATTCC 720 AGCACAAGCT ACAAGCGCCC CACTCGGCAC CTTCCTCCAC AGGCAGCCCA CAGCGGGGCT 780 GGAGGTAGTC AGCTGGGGAG TTAGCCTAAG GCTCAGTGAG TGGCTCTGCC CACAGGTGTG 840 TCCTGGGACC TGTGTCCAGC TGGGGCTGGG GAAGATGGCC TGTGTGGGGG TGCTGAGCCC 900 GAGCCTGCAG CGATGGTGAG GAGCTGAGTG CTAGCTGGAA TTCCACAGGG TGGCTCCTGG 960 GACCCACAGG GGCAGCTCAG AGCCTGGAGG ATTTGCTCCC ACCATGGGGT GGAGAAGGGG 1020 CAGCAATGTA TGCATGTATG GCTGGGTCGG GGGGGCGGGG GGTCTCTTAA AAGTTCCCGC 1080 CTCCTCAGGT TTCAGAGCTG GCTGGGTACG CGCTTCTGGT CAGCGAGGGG CACCAGCACG 1140 CAGCGACAGG GGGTGCGGCC CGCACACGCA GCATGCCGAC AGTGGGCAGG TGGCCACCAG 1200 GCGTGCCTAA GAGCCCCGGG AGGAGGGGGG CGTGTGCAGG GCCAAGGGAG GTGTGAGCCT 1260 AGTTTTGGTA GCGACGAAAT CAATCCGTAC ACAAACCACG TTCCAAACCT TTCTTGCGCA 1320 GCAGCCGCGC ACCCCTGGGA CTGACACCCG GAAGGATGCG AGGACTGGGT CCCCGCATCC 1380 CCCTGGCAGC CCTGGCAGGA CCCCATCCTC GGCCCCGCGC CCACTCCGCT 1430
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