Tag | Content |
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EnhancerAtlas ID | HS177-18998 |
Organism | Homo sapiens |
Tissue/cell | SK-N-SH_RA |
Coordinate | chr6:3247290-3248480 |
TF binding sites/motifs | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
FOSL1 | MA0477.1 | chr6:3248079-3248090 | GGTGACTCATG | + | 6.62 | JUND | MA0491.1 | chr6:3248079-3248090 | GGTGACTCATG | + | 6.02 | REST | MA0138.2 | chr6:3247715-3247736 | CCCAGCACTCAGGACAGTGCC | + | 6.6 | TEAD1 | MA0090.2 | chr6:3247563-3247573 | CACATTCCAT | + | 6.02 | ZEB1 | MA0103.3 | chr6:3248162-3248173 | CCCACCTGCCC | + | 6.14 |
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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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| Number: 1 | ID | Chromosome | Start | End |
GH06I003246 | chr6 | 3246856 | 3249920 |
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Enhancer Sequence | GTAGTGAGCT ATGATCACAC CACTGCACTC TAGCCTGGAC AACAGAGTGA GACCCTGTCT 60 CAATTTGGAA AAAAAAAAGG TGCACTGACC ACGGGTGTCC AGCATTCCAG AAGCCCACTT 120 GGTGTTCTCC TCATCTCCTA CCCCAACAAG CAGCTACTGC CTTGCCCTCC AGCAGTAGGT 180 GTTAGCTCTG CAGGCTTCAG GAGTTGATAG AAATGGAATC CGACAGTATG TACTCCGTGT 240 ACATTCTTTT TGTGAGACTC ACCCGTGTTC TCGCACATTC CATAAGCATC CCATGCATTC 300 CTAGCTCCTT TAGATGCTGT GAACTGGGGA CGGTTGACTG TGTCGTATTT ATGTGTGTGT 360 CTGCCTCCCG GTTCCAGCGG AGGGCGAGGC GGGGGTCATC GTTCTGAAGG GCATCTTTGT 420 GTCTTCCCAG CACTCAGGAC AGTGCCTGGC ACACAGATGC TTCAGTAAAT GTTTGCCGAG 480 TGAACCCGAT GAATGGGCAT TTTGTCACTG GGTCTTTTCA TTTATTCCTT GGCTTGCTCC 540 CTGTCTCCCC TTGAAACACA GCTGCTTTCA TTGACCGCGT CTTTATTTGT TGGGTGGATG 600 TGCTTGTTTT CAGTGCCAGG AAGGAAAAAC AAGCACAGAA GTCGCCCCTC CCGGGCAGCC 660 ATATTCCCGG CTAAGAAGCC CTCCTTTGTG CCAAGAGCAG AACCGTCTAT GGCTGGGTGG 720 AGGGTCACAG CCTGTGGGAC GGTGCGGAGA GGCAGGGGGG TGCGGCGAGC TCTGGGCTTG 780 CAGGCAGGCG GTGACTCATG CAGAGTCCGG CCACCGGTGC GGGAAAAGGG CTTTGACGTT 840 CTCAGCAAAA CCCCAAGGCG AGCTCCGAGC AGCCCACCTG CCCCTCCCAC CCACGCAGGG 900 CCTTGCAGAT GAATCTGCTT CTGTATCACA TGATCCGTTT CAGCAGGAGA GAGACGGAGA 960 GAAACAGCCT TTTGTTCTGC CAGCCTCCAT GATTGCGTAT CTTAGGCACA ACGCTCTGAA 1020 GTCAGGCTGA GGATTCTAAT AAAACTTGGG AAGCTTTACC CGGAAGACAA GGTGCTCTTT 1080 CACTAGGCAT GATTTGGACC CAGGATATAA ATTCTCTTTC GTGGGACGGG AGAGTTGTGT 1140 CTTTGCTTAT CCTCGGGGAG TCTCACTGTG CCCCACTGAT CATGCGTGCC 1190
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