Tag | Content |
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EnhancerAtlas ID | HS028-03251 |
Organism | Homo sapiens |
Tissue/cell | Colo829 |
Coordinate | chr6:3247310-3248630 |
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 | TBXT | MA0009.2 | chr6:3248510-3248526 | TCACACATATGTGCAA | - | 6.48 | TBXT | MA0009.2 | chr6:3248510-3248526 | TCACACATATGTGCAA | + | 6.49 | 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 | CACTGCACTC TAGCCTGGAC AACAGAGTGA GACCCTGTCT CAATTTGGAA AAAAAAAAGG 60 TGCACTGACC ACGGGTGTCC AGCATTCCAG AAGCCCACTT GGTGTTCTCC TCATCTCCTA 120 CCCCAACAAG CAGCTACTGC CTTGCCCTCC AGCAGTAGGT GTTAGCTCTG CAGGCTTCAG 180 GAGTTGATAG AAATGGAATC CGACAGTATG TACTCCGTGT ACATTCTTTT TGTGAGACTC 240 ACCCGTGTTC TCGCACATTC CATAAGCATC CCATGCATTC CTAGCTCCTT TAGATGCTGT 300 GAACTGGGGA CGGTTGACTG TGTCGTATTT ATGTGTGTGT CTGCCTCCCG GTTCCAGCGG 360 AGGGCGAGGC GGGGGTCATC GTTCTGAAGG GCATCTTTGT GTCTTCCCAG CACTCAGGAC 420 AGTGCCTGGC ACACAGATGC TTCAGTAAAT GTTTGCCGAG TGAACCCGAT GAATGGGCAT 480 TTTGTCACTG GGTCTTTTCA TTTATTCCTT GGCTTGCTCC CTGTCTCCCC TTGAAACACA 540 GCTGCTTTCA TTGACCGCGT CTTTATTTGT TGGGTGGATG TGCTTGTTTT CAGTGCCAGG 600 AAGGAAAAAC AAGCACAGAA GTCGCCCCTC CCGGGCAGCC ATATTCCCGG CTAAGAAGCC 660 CTCCTTTGTG CCAAGAGCAG AACCGTCTAT GGCTGGGTGG AGGGTCACAG CCTGTGGGAC 720 GGTGCGGAGA GGCAGGGGGG TGCGGCGAGC TCTGGGCTTG CAGGCAGGCG GTGACTCATG 780 CAGAGTCCGG CCACCGGTGC GGGAAAAGGG CTTTGACGTT CTCAGCAAAA CCCCAAGGCG 840 AGCTCCGAGC AGCCCACCTG CCCCTCCCAC CCACGCAGGG CCTTGCAGAT GAATCTGCTT 900 CTGTATCACA TGATCCGTTT CAGCAGGAGA GAGACGGAGA GAAACAGCCT TTTGTTCTGC 960 CAGCCTCCAT GATTGCGTAT CTTAGGCACA ACGCTCTGAA GTCAGGCTGA GGATTCTAAT 1020 AAAACTTGGG AAGCTTTACC CGGAAGACAA GGTGCTCTTT CACTAGGCAT GATTTGGACC 1080 CAGGATATAA ATTCTCTTTC GTGGGACGGG AGAGTTGTGT CTTTGCTTAT CCTCGGGGAG 1140 TCTCACTGTG CCCCACTGAT CATGCGTGCC TTCCAAAGCT GTCAGGTAGC CCCTCCACAA 1200 TCACACATAT GTGCAACCAC ATATTTTCCA ACCCAAACGA GGGTACACAC CATCTGGGGA 1260 GGGATTCCCC CTTCCCATAT GCGTGAATTC GTTTAGCTAA AAAGCATTAA CAGTCACAAA 1320
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