Tag | Content |
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EnhancerAtlas ID | HS052-19881 | Organism | Homo sapiens | Tissue/cell | Fibroblast_foreskin | Coordinate | chr2:26107890-26109470 | TF binding sites/motifs | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
FOXA1 | MA0148.4 | chr2:26108960-26108976 | CACTAAGCAAACAAAT | + | 6.43 |
| | Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder | Number of disease enhancers: 1 | Chromosome | Start | End |
| | Number: 2 | ID | Chromosome | Start | End |
GH02I025885 | chr2 | 26108441 | 26108475 | GH02I025886 | chr2 | 26108901 | 26109090 |
| Enhancer Sequence | CTTCCTGTAC AGCCTGTGGA ACCACGAGAC AATTAAACCA ATTTTCTTTA TAAATGACCC 60 AGTTTCAGGA ATTTCTTTAT AGCACTGTAA GAACAGATTA ATACAAGGTG CAAGATGAAA 120 ATGGACTTCA CCAGCCTTAC AGTCCCATTC AAGAATAGCT TTGAACAACA GGAGTGAAGG 180 GACAGCCTTC CAATGTGCAG AAGTTCAGGC AGTGTACTGG ATTATCTACT TTGTGTGGAA 240 AGAGAAATGG CCCAAGGTCA GAATATAAAC GGATTCATGG TAGGTGGAGA AGAGCTCAGC 300 CAAGTGGTCG GGGTCATGGA ACAAAAAAGA CTATAAGATC AGAGGTAATG AGGTTGGGAT 360 AGAGATATGT GGATGAACCT ATGAACACAA AATATGAAGA TCTCATGTTT AATGCTCATA 420 TTAATACTCA CCAGAAAGCG TAGAATAACA TTGGCTGAGT ATGGTGGCTC TTTGAAAGGC 480 TGAGGTGGGA GGATCACTTG ATGCCAGTAG TTTAAGACCA GCTTGGGCAA CATAGCAAGA 540 CCCTGTGTCT ACAGAAAATA ATGTGGTTTT TTTCTTTTTT TTTTTCTTTG AGACGGAGTC 600 TCGCTCTGTC GCCCAAGCTG GAGTGCAATG GCGTGATTTT GGCTCACTGC AACTTCTGCC 660 CCCTGGGTTC AAGCGATTCT CCTGCCTCAA CCTCCTGAGT AGCTAGGATT ATAGGTGCAT 720 GCCACCATGC CTGGCTAATT TTTGTATTTT TAGTAGAGAC GGGGTTTCAC TGTATTGATC 780 AGGCTGGTCT CAAACTCTTG ACCTCATGAT CCGCCCGCCT CAGCCTCCCA AAGTGCTGGG 840 ATTACAGGTG TGAGCCACTG TGCCCAGCCA AAAATAATAT TTTAAAAATT AGCTGGGCAT 900 GGTGGCATGC GCCTGTAGTC CCCACTACTC AGGAAACTGA GGCAGGAGGA TCAGTTGAGC 960 CCAGGAGGGT GAGGCTGCAG TGAGCCATGA TCACACCACT GCATTCCAGC CTGGCTGACA 1020 GAGTAAGACC CTGTCTCAAA AAAAAAAAAA AGCATAGAAG AAGCATGAAG CACTAAGCAA 1080 ACAAATAGGC AGAATGACTC AGTCAGTTAA CATCAGGCAG ACTCTGTCAT TGACCACTGC 1140 GGTGGTACAT AATTCATCTA TGAACATAGT AGACATGGTG GCAGGAATGG AGGCTACAAA 1200 TGGACCCAAC ACCGTGGGTT CCCACTCACC ACTGAACTTT TACCTACTAC TGCTACTGAA 1260 TGTCCAATCT GCCAGCAAGA AAGATGAAAA CCAACCCCCT GATTTGACAC CATCCCTCAA 1320 GTACACCAAT CAGCCACTTG GAGGTAAGTT GCCTACAGTG GACCCCTTCA CCTTACAAGG 1380 GGCAGCAATT CATTTTAACT GGAATATGCA TCTATTTCAG GTATGAGTTT GCCTTTCCTA 1440 CTAATAGAGC CTCAAAGTGT GCTCAGCCAG CACCACTTTC AAGAGCTTAC AAAATATTTG 1500 CTCCATTGAT AAGGGATCTC ATATAACAGT GCATCAAAAC AAAGAGCCCT TTTTTTTTTT 1560 TTTGAGACGG AGTTTTGCTC 1580
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