Tag | Content |
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EnhancerAtlas ID | HS139-21973 |
Organism | Homo sapiens |
Tissue/cell | Myotube |
Coordinate | chr17:228660-230080 |
TF binding sites/motifs | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
Foxd3 | MA0041.1 | chr17:228669-228681 | GAACAAACATTC | - | 6.14 |
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| Number of super-enhancer constituents: 1 | ID | Coordinate | Tissue/cell |
SE_65261 | chr17:229435-230303 | 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 |
GH17I000379 | chr17 | 229436 | 230303 |
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Enhancer Sequence | TCTCACCACG AACAAACATT CAGACTGTGT ACGATCTTTC ACCACCACAG ACCGTCACAA 60 AGGCTGTCCC AGAAGTTGTC ACCTGTGCAC AGGTGCCAGC ATTTCTTTAG GGTAGATCCT 120 GAGAAGTAGA ATCACTGAAT CACTATGTCA CAGGGCAGCT GCATTTATTT TAACAGTTCT 180 CACCAAACTG CATCCACCAT GATGTTCCTT TCCAAGCCTC GGATCCCAGA GATTTACAGA 240 CCCCATCTCT ATGATATGTC TCCTTGTCGG CTTCAGCCAG GCATTCATAC CTCCCTGGGA 300 TACTCCAGGC CTCAGTGCAG CTCTGTGGCT CCTCCTTACT ATGAAAACCA TCACCCACCC 360 CGAGACAGGC TGCCGACATC ATCGGCAGCC TTGGAGCACA GCCCAAATGG TCGCCCATCC 420 GGCTACTGGT GGAGAAGACT CTTGGATGAG GAAGGCAGGC CTCCTAACTC TGAGATGCTG 480 CACCTCTGTC AGTCAGGGGG TACTCCATCA CTCCATCCAT GAGTGAGAAG GAGGGGCTGG 540 GCAAGAGGAG ACTAAATCCT GGCGTCACTC AACGGCTTGG ATGGGCCAGA ACCAAAGATG 600 AAAATGCACC AACATGTAAA TTTAGCCATG AGCACAGCTG GGTGATGGAG ACAGGACCGG 660 ATCGTCAGTA TCCAACACGC AACTGATTAA GTGTCCATGG TAAAATAAGT GCTCTTACAC 720 GAGGTGCTAA CGACGTAATT GCGGTCTTAC ATAAGGTGCT CTGGTATTTT CAGCAGCAGA 780 TAACTGCCAT GTGAATGGAG AAGCCGCCCT CCCAATGAAT GCTGCTTACT GTACAGGCTG 840 GCACAGGCCT TGAAATGCCA GTGCTTTGCA GGCAGCCAGC TGCTGTCAGA GGGGTGAGGA 900 TGTCTGTGCC CGGGGCTGCA GCTCCGCTCG TGTTCTGCAA TTTCTACAGG CTGGCCGGAC 960 TCCCCACAGC CAGCTGGGGG TACACACATC ACCGTGCTTA CACCCCCAAG CATCCCAAAA 1020 GCAAGGAAAA GGGCCACTTC AGGGGCTCTC CCAACCCAAG CAGCCACCTT GTAGCTAAGA 1080 GAGCTCTCCC CAGACCCAGC AGGGTGGAGG TAGACAGGAA GAAACCAGAG CCAGCCCGGG 1140 CTCAGCTGCC TCGTTCCCAG AGCTGACCCC TCCGGAGCCT AGGTGCTCAC CCTCATGTCA 1200 CCTCCCACCT GTCACGAGAA ACCCAAGGCT GCAGGTACAG TGAAGTCAAA GTGGCCTCTT 1260 GGAATGGTGT GTCTGTATTC ACGTCCCGGG TTTAGGATCC CTGCAGCCTT TTTTCCTGTT 1320 TCGCTCCATT GTATTAAGTC TAACACATAC ACAGAGGAGT ACACACATGG AACGGGTAAG 1380 CGTTGGCATT GATGGAAAGA ACGCAGCCCT CTGACTGACA 1420
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