Tag | Content |
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EnhancerAtlas ID | HS098-23407 |
Organism | Homo sapiens |
Tissue/cell | HSMM |
Coordinate | chr17:17280420-17281880 |
TF binding sites/motifs | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
FOSL1 | MA0477.1 | chr17:17281853-17281864 | GGTGACTCATG | + | 6.62 | JUND | MA0491.1 | chr17:17281853-17281864 | GGTGACTCATG | + | 6.02 | TCF3 | MA0522.2 | chr17:17281163-17281173 | AGCAGGTGTT | - | 6.02 |
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| Number of super-enhancer constituents: 1 | ID | Coordinate | Tissue/cell |
SE_65490 | chr17:17280362-17282763 | Pancreatic_islets |
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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 |
GH17I017377 | chr17 | 17280363 | 17282763 |
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Enhancer Sequence | AAACCCAGTT TCTATTCATT TATACAGGAG ACTCTGTCCT CCTGCCTGTG CTCTACCGCC 60 CGGGGCGCCG GGCACCTCTT TTTTATGAGT TGCTCTCTGC CTTCCAGTAA GCCAGCAGCT 120 TTCCACGGAA GTGCCTTGGC TTGAGAGAGG CCTGCAGAAA CCAGCAGGGA CAGGATCTCT 180 GAGAAGTTCC CCAGCAGCCT GAACATCGGA GCCACTGATC TTCCAGATAA ATAGGGGCAG 240 ACAAAGGCGA GTGAGCAGTG AGCTCCAGAG AAACCAGTTG TGTCCGGCCG CAAAAATAAT 300 GTCCCTGGCT GCAAAGTGGA CTCAAAATGG ACTAATAGGC AATTAGCACC AGAGTGCCCC 360 TACCCAGCCC GGAGCCCATT AGACGCAGGA CGGCTTTAAC CAAATCCTGT CTTAAAGAGC 420 TCTGTTGAGA GTCTCCATAA TGTAAGTAGG GCCTTAATGG GGAAAAACAG CCTGGTGACG 480 CAGGTGAAGA GAGCGGTTCT TAGTGGGAGC TTATAAGTGG GCTGGAGGCA GCCGAGCACT 540 ATTGAGGTGC TCTGCAGGGG CAGGTGGAGG CAGAGGCGGT TGCGTTTCAG TCCAACCTGT 600 TCTGGTTAGC TCTGTTCCAG GGCTTCCGCC TATCCCCAAA TCTCTTCCAT ATTTGGAGCC 660 CAGAAGGGCA CCACCGCTGT GGTGTAACCT GCGTCTCCAC CTCCGCCCAG GGTGGTCAGA 720 TCTGGTATGT TCTGGGGACT GGAAGCAGGT GTTCAGGCTC CAGGCCTGCA TGTGTCTGTG 780 ACACTGGCCT TGGCCCTGTG CCTTGAGTTC CCTTCCCTTT ACTCTCTCCC TCCCTGGTGA 840 GGCGAGAGTA TGGCTGACAT CACCTACCCT CTGGGCAGCA CCTTAGGGTC TCACCCCTGG 900 CTGCCTGCGG GAGCCACTAG GTGAGCTTTC CAAATGCTGA TGCCCAGGCA AGATCCTGAG 960 ATTCCAATCG GTTGGTCTGG AGTGGGGTCC CAGCATGGGG ACCGTAAAAG CTCACCCACT 1020 GGCTCATGTG CACCCAGGGC TGAGCCCCAC TGGTCCCCAG GGCCTGTCCC GTTCATGCCC 1080 TCTCTGCTGG TTAGCCAGGC CCTACAGGGA ATTAGGCAGG TGTACCTTAT TAGATCCCAT 1140 GCTTGAATGA GACACCTGGG TAGCCTCTTA GACCCTGGAG CAGGAGCCCT CAAGCGGGTT 1200 CCCAGACTGG CAGCATTGGT GAAATGCAGA GTCTCAGGCT CAGCCCCAGA CCTATGAACT 1260 AGAATCCCGC AGGTGGGGTC CAGCCATCTA AGTTTTAACC AGCCCTCAAA TTTGAGAATC 1320 ACTGTGCTAG AATAGTGACA GAATTATCAC CGCAGTTCAG TGCTTTTGAA ACTTTAACAT 1380 GGACAGAACT CATCTGGGCA TTGTATTAAA ATGTAGATTC TGGGGCTGGG CGCGGTGACT 1440 CATGCCTATA ATCCCAGCAC 1460
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