Tag | Content |
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EnhancerAtlas ID | HS073-13638 |
Organism | Homo sapiens |
Tissue/cell | GM19238 |
Coordinate | chr7:149193340-149194600 |
Target genes | |
TF binding sites/motifs | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
Nr5a2 | MA0505.1 | chr7:149193455-149193470 | GCTGTCCTTGGACTC | - | 6.15 |
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| Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder | Number of disease enhancers: 2 | Chromosome | Start | End |
chr7 | 149193399 | 149193541 | chr7 | 149194138 | 149194526 |
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Enhancer Sequence | CTGATGGGGC CAGGAAACCC TGTGTAAGGT CTTCACACTA TGTGGTGGGA GGTGGCGACT 60 GTGCGCTGCT CACTCCAGCC CAGCTTCTTA CTGACAAGTG GCTGGAATAT GTGGGGCTGT 120 CCTTGGACTC CTGCCAGGGG AGCTGAAACT CTTTGCTTGA GAGGAGCTGA TGGTAAGAGG 180 AGCCGGATCC CTCATCCACT GCCCACCCGC AGGATGAAGT CCAGGCATGC AAACCCCTTC 240 TTAGTCTCTC TCTGCAGACT CCTTTCCCAC TGCCTCCAAA CCAAAACCAT CTTCTCCAGG 300 CTCATGGACT CCTTTCTGTG CCTGCACACG CCCTGCACTG TCCCGTCTCT CTGCGCCTTT 360 GCCCAGGCAC TCCTCCCTCC CTGAAAGCAC CACCGGTCTA GCTGGGCCTG AAATCCTAGC 420 CTTCCCTAAA AGCCCGGCTC AAATCACAGA GGCGCAGAGC ATCAGGCCAG GAGGGGTGGA 480 CAGCGGTACC AAGAGGCCCC CTGACACTCC TTCCCCCGGA GCCCACCGCA AGCTTCCACC 540 TGGGCGCCAG CACTCACCCC TTTCTGTTTT GCACGATTAT TGCCCGCGTA CCTGCCTGCC 600 TGGTCCTTGA ACACACAGCC ACTGTGTGTC TTTTCACACT TTCCAGCTGG GTAAGCCTGG 660 GCAAGTTAAG TTCTCTAGGC CCCGGGTTTT TCTTTTGTAT GACAGAGATT AACACCAGTA 720 CCCATCCCAC AGGCTTGCTG TGAGGACAGA CTAACGCCTC AACAGGGCTT GTGGAAGTGC 780 GTGGCTCTAT ATTCCCTTCC GCGCCGACCC CGGGAAGCTG GGCACGTAGT GGGAGTCGGT 840 GTATGCGGAT TCGAAGCCGG ACACCTCCCA GGTGCCACCA GGCCGCTGCG GGGGAGATGG 900 AGAGGGACCT ACAGGCCGAG CGCCAGGCAG AGAAAGGAGC CGCGGGTGGG GGGGCACCCA 960 GAAGGAGGGG ACAGCGGCTG GGGCGGGGGC AGGAAGCCCC GGAGGGCCCA AAGAACTTGG 1020 CGTGGGGCGG CCCGGGGCGG GGACAACCGT TCCGCCAGCG CTCGGGTTCG GCTCGGAGTG 1080 GGGGCCCGGC CGACGGGCGC AGTAGGCCCC GGCGGACCCC GCGCCCCATT CGCGGGAGCC 1140 CCAGGCCCGG TGGTCCGGCC CGGACCCCGG AACCCCTCCC CAGGGCCTGC GGCGCCGTGT 1200 GCCGGGGCCG GGCCGCCTGG GGCCCCCAGG CCGCGAGTCC CTGCGCGCGC GGGTCGCCCT 1260
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