Tag | Content |
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EnhancerAtlas ID | HS053-07186 |
Organism | Homo sapiens |
Tissue/cell | Foreskin_keratinocyte |
Coordinate | chr11:57016330-57017790 |
TF binding sites/motifs | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
ALX3 | MA0634.1 | chr11:57017695-57017705 | TTTAATTAGA | - | 6.02 | CTCF | MA0139.1 | chr11:57016687-57016706 | TGCTGACCTCTGGTGGAGA | - | 6.04 | CTCF | MA0139.1 | chr11:57017374-57017393 | CAGCGCCACCTTGTGGCTT | - | 6.7 | HNF4G | MA0484.1 | chr11:57017521-57017536 | TGAACTTTGCACTGA | - | 6.13 |
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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 |
GH11I057248 | chr11 | 57016415 | 57017477 |
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Enhancer Sequence | TAGTTCCTTG AAGTGTGGAA CGTGCCTGCC CTGCCTGCCC GAGGCTTTGA CAGAAGCCAG 60 TGGGATAGTC AACAGCTTTG TGTGAGCACA GAGAGAGGTA GCTGCCCCAG ATGCTGCGGG 120 GCTCTGCTGA TGAATGACCC ATCAGTCCCA CGGGTCCCAC AGGTATCCAG CGGCAATCTA 180 CCCTTGCCAA GAAGGCACAA CACTAGTGCT ACAGCATCTC CCACTCTTAG GACTGCTCGG 240 GCCCTAAGGA TGGTTGGGGA GGTGGAAAGA AGAACTGGAC ATGGGTGAGC CAGCTCAAGC 300 ACAGAGCTGC CTCCTGAGCC TGGCTGTTTG GCTGCTGTGC CTCTGATGGC TCGGTGATGC 360 TGACCTCTGG TGGAGATGAG CTGCTACTCA GCTTTGACCT CCCTCTGAGC ACCAGGAGTC 420 CCAGCACTGG CTTCCAGCCC CGCCACCGGG ATGCAGACCC AGCAGCCTGA GACCCCAGAG 480 GGTGCACCTA AGCCCAACCT CTCTCCTTAT TCCAGGGCCC TGTGGTATCT GGAATTGTCT 540 ACCCTGGAAC CTTATGGCTC AGGGGCTAGA AGAACCCTTA GCAAAAGGAA CTTACCCAGC 600 TGATGATTCT GACGCTGAAC AGGCGCTAGA ACCCAGCACA GGTCCCAGTC TCTTGGAGAA 660 TTAAGGCCTC GGCCTCTCCA CCTAGTTCAG TGTTTTGAGC TACACATTCT CTTCTGACAT 720 GTGGTTACAC CGCACTGTAA TAATACATGT TATGACACTG ATATAGAAAA AGAAATGTTC 780 TTGTCTAATT ATTTTCTGTT TGGGTGGTGC AGAAGTAAAA CCAAGAGACG TTGAATCATC 840 CTCAGTATTA TTCATCACTC TTCCTCAAGC ATGTCACTCT GTAAAGACAA CATATGAAAG 900 GGAAAATGTT ACCCTGTTTT ATTAAGGAAA ATTATGGACT AGAAAAAGAC TGCTTTTTTT 960 TTTTTTTTTT TTTTTAATAA GCTGACATTG ATAGAGAAAA GTTGAGCCAA ATCTCTGGAG 1020 GCAGGAATCT CATTGCTGAG CACCCAGCGC CACCTTGTGG CTTCTCGCAG GACAGCGATT 1080 CCAGCTTCCA CTCATTTCTC TACCCACCAC TAAAAACATT TATTGAGCAT TTCTTATGTT 1140 CCCTTTCACC TGTTTCTCTG CTGAGCCTCT TATCTGAATC TTTTATCTCA ATGAACTTTG 1200 CACTGAAATC TCTTTCGATA CACTCATTAA TTTTAGCATG GGAAAAAGGG TGGCTACACA 1260 GTTGAGTTGG CCCACATAAG AAGGTGTCTA TGGAGATATT CTTTATCCAT GAGCCCTCCC 1320 AGTTATTCCA ATGTCAGCCC TGGGACCCTG AAGATCACTC ACAGATTTAA TTAGACAAAT 1380 CTCTTAAAAT ATGTGTGTAT ATTTTCCTTT CCCTCTTTCT CTTTCTGGAA ATACGTTTTC 1440 CTGTTTCTCA GGCAGCAGCC 1460
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