Tag | Content |
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EnhancerAtlas ID | HS179-06070 |
Organism | Homo sapiens |
Tissue/cell | SkMC |
Coordinate | chr11:8884870-8886330 |
TF binding sites/motifs | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
BARHL2 | MA0635.1 | chr11:8885936-8885946 | ACCGTTTAGC | - | 6.02 | EBF1 | MA0154.3 | chr11:8885408-8885422 | ATTCCCCTGGGACT | - | 6.33 | EBF1 | MA0154.3 | chr11:8885408-8885422 | ATTCCCCTGGGACT | + | 7.17 | Nr5a2 | MA0505.1 | chr11:8885006-8885021 | CCTGACCTTGAGATC | - | 6.34 |
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| Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder | Number of disease enhancers: 2 | Chromosome | Start | End |
chr11 | 8885040 | 8885154 | chr11 | 8885910 | 8886000 |
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| Number: 1 | ID | Chromosome | Start | End |
GH11I008863 | chr11 | 8884948 | 8886628 |
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Enhancer Sequence | TCGGCTCACT GCAAGCTCCA CCTCTCAGCC TCCCCAGCAG CTGGGACTAC AGGCACACGC 60 TGCCACGCCT GGCTAATTTT TTTGTATTTT TAGTAGAGAA GGGGTTTCAC CATATTAGCC 120 AGGATGGTCT CTATCTCCTG ACCTTGAGAT CCGCTCGCCT CGGCCTCCTA AAGTGCTGGG 180 ATTACAGGCG TCAGCCACTG CGCCCGGCCT GCCTCTTACG CCACTTCCTA TGCAAACACT 240 GTGGTCCTGA GTGCTATTCT AATTCAAAAG AGTGACCTGT CAATGTACAA ATGGGGGAAA 300 AATAGCAAAA CGGAATCCTC ACAACTGATA TTGCTGATTA ACTGGACAAG AAGGATTCAA 360 TTAATATACT TTGACCTTAA GTGCCATTTT TCCATGTTAA CCCACAGCAC CAAATACTCA 420 TTTGCAAGTT GGGTTTTCTT TATCTCCAGG TATCTATGTA CAGATTCGAG TGACTACTGA 480 AAAGTACAAA GCTTTGATTC CCCTCCCATA CAATTATACT ATTTTCAAGA GAATTTCCAT 540 TCCCCTGGGA CTTGGACCCA GTAGAAGAAG CCTTTTGGGT CTAAGTACTT AGAATGCACT 600 CATCCCTGGC TCAAGAGGCA AGACCAGACT TTCAAGAAAA GCTTCTCCAG GCAGTCCTGG 660 AGAAAGACAG CTATTGAGTG GCACTTCCTA ATTCAAGGGG ATATTATGCT AACTAGAGTT 720 CCCGGCAACA GTAAATGTAA TCCAACATGA CTAATAGAAA AAATAACTGA CTAGGCCCTG 780 TTTACTCACT AGAAAATATA TCCCCACATG ATGAGCCTTA ACAGAGGTCA TCTCAGCTTC 840 CAGAGACCAG AGTGTTGTAA AAACAGTTGC TTCCCAACAG CAATATTTGG ATCAGGAGGT 900 ACCCAACACT CATATCCAAA ACTAATTTCC CATCCAATTT CTTTTGTTGT TGTTGTTATT 960 TTCACTCAGG GGCTCACTCT GTTGCTCAGG CTGGAGTGTA GTGACACAAT CTCGGCTCCC 1020 TACAGCCTTG ACCTCCCAGG ATCAAGCAAT CCTCCCATCT CAGCCCACCG TTTAGCTGGG 1080 ACCACAGACA CGCACCGCCA CGCTCGGCTA ATTTTTGTAT TTTTTTCATA AGGACAGAGT 1140 CTCACTGTGT TGCCCAGGCA GGTCTCAAAC TCCTGGCTTC AAGCAATCCT CCCAATTTGG 1200 CCTCCCAAAG TGCTGGGATT ACAGGTGTTA GCCACCAGGC CTGGCCTCCA TCTAATTTCT 1260 TAACTTCATC CACTCATTGA TTCATCAAAC CCCTAACATT AAGCATATTC ACTGAAGAAA 1320 GGTAATAAGA GAATAAACAG ATGCCCGTAC ACACCCCAGT GCTTTTTCCG CAGGAGATAT 1380 TCAAAAACTA TAGGACACAA GAAAGGAAAA GTATATAAAT GATAGTGATA CAGAGCACTT 1440 CCCAGAGACC AGTGTCTGAC 1460
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