Tag | Content |
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EnhancerAtlas ID | HS026-20750 |
Organism | Homo sapiens |
Tissue/cell | CNCC |
Coordinate | chr20:57044040-57045240 |
TF binding sites/motifs | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
HSF1 | MA0486.2 | chr20:57044550-57044563 | GAAAGTTCTAGAA | - | 7.04 | Myod1 | MA0499.1 | chr20:57045159-57045172 | AGCAGCTGCCCCC | + | 6.03 |
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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 |
GH20I058469 | chr20 | 57044413 | 57048075 |
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Enhancer Sequence | GTCAGAGCTA ATGTGTCTTT AATGCCAACC TCCCTGTTCT CCCAGAGAGA GCAACTTAGA 60 ACTTCGGGTT GGCAACAGAT CTACAGAGGA TTTATGTTGT TTTGTTTTCA TGGAATTTAA 120 TTTTACAGTT ACCTTTAATT TATGACAAGT GGCTCTGCTC CCCATATCCA GGATAATATT 180 ACGTTTTCTT TAAAAATAAT CACATTACAC TGTCAATGTA TGCCAATTAT ATCTCAATAA 240 AGCTGTAAAA ATAAATGAAT ATATTTTAGT AAATAAAAGC AAGTTGGTTT ACAGAAAATG 300 ATAAGTAAAT ACTAGTATAG GTACTTAAAA ATAGGGAGGG GTGAGCCACA CCCCTGAGGG 360 TCTCAGGCCT GGAGAGGGGA GATTTGCCAG GAGGACACAG CAGGTCACAC TGGACCTCTT 420 GATGGTTCCC AGGCTCTGGG GCCTTTCCCA CTCTTCTCCC AAGAAGCAGC AAGGTCAGTC 480 TGGAGAGCAT GGCAGGGAAC TTTCAAGGAA GAAAGTTCTA GAAGAAATTT CTTAAAAGAA 540 CTGCTCCAGA ATGTTACTGT CTTGGGGCAG AAGCAGCCTA CAACCAGCGT CCCCCCTTCC 600 TGTACCCCAG TTCTGTCTGG GTGACCCTGG TGAGTGGATG CCTGGATCTC CCCTGGACTG 660 TGCCGTGGGC GTGGGGGCTG TGTGCAGCCT GGCTGAGCCT GCAAATGCAT TCGAAGTGGC 720 CTCGAAGGAC TCATGTCCCC TTCCTCCAAC GAAAGCGCTA GCAGATGTTT GGCAGTCGGG 780 AGTTTCTGCC TGACCTCAGG AGGTACAGGA AGGACACGGA GAGGCCAGTC CTTGACCCCA 840 GAATGGGACT GGCCTGGAGG GGATGTCGGG GGAAGGAGGA ATATGCCAGG TGTGAAGGGG 900 GCCACAGCCT CCCTTTTCCC CGATCCCTGC CCCAGGAGTG GGACTCAGCT GGCTGCTGTA 960 GGGTTTGTGC ACCACAGATG AGGAGAGAAT GCAAAGTCCA TTGGCCGCAA AGCAGCGACT 1020 GAGCCTCTGA AATGTCGAGT GAGCCTGTCA GGTTAGACAG AATTAGATGG GTGCACCCAG 1080 GCTCTCCCTG GCCTGCCACT TCCCGCCCCA GGGCCCTTCA GCAGCTGCCC CCTCTGCCTG 1140 GCTCTTCCCT GGCTCTCTAG ATGGCTGATT CCTCTCCTTT TAGCTCTCAG CTGATGTCAC 1200
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