Tag | Content |
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EnhancerAtlas ID | HS081-08099 |
Organism | Homo sapiens |
Tissue/cell | HACAT |
Coordinate | chr17:4150870-4151920 |
TF binding sites/motifs | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
FOS | MA0476.1 | chr17:4151109-4151120 | GGTGACTCATT | + | 6.02 | Klf1 | MA0493.1 | chr17:4151503-4151514 | GGCCACACCCA | + | 6.62 |
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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 |
GH17I004246 | chr17 | 4149624 | 4152890 |
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Enhancer Sequence | ATAATGGAGG AGTGCTTATG GCTGAGACAT TACCAGCCCG TGGGGAATAC TGTCTGCTTA 60 CAAACAGCAA TGCAAATGTG TCCTTGAAGT GTCACCAAGC TGTACAGTTC TTACAAGAAA 120 AAGTACAACA TTATTCTGAG CAAAATGGAG AGAGAATTTA CAGTGTGCAG GTTCTAGGGC 180 CAGACTGACT GGGATCAAGC CCAGCCCCAC TACTGCCTAG TTTTGATACA CCTTAGGCAG 240 GTGACTCATT CTCTTCACCT GCAAGGATGT TGTAAACACT GAAAGTACTA ATACATGTAA 300 TAACCTTAGA ATACAACCTG CTCTGCAGTA GGTGGTCAAA ATATATTAGC TATTATTACA 360 ATTCTTAGAA AGGCAACCCG GGGTAGTCAG TCCTGTGTTG CAAGATTCTC CCTGCACACT 420 GATAGCCCAG AGCTCGCATT CCAGAGTCTC ACTGACTGGG TTTGACCCCA GCTTACCCAT 480 TTACTAGCTG TGTGACCTTG GGCAAGTTAC TTACTTCCTC TCTGTGCTTC AGTCTTCTCA 540 CATGGAAAAT GAGACTAATG ATACTATCTT AGAGCAGGTG TCCCCGACCT CCAGGCCGTG 600 GACGGGTACT AGTTTGTGGC ATGTTAGGAA CTGGGCCACA CCCAGCAGGA GGTGAGCTGC 660 GGGCGAGTCA GCATGACCAC CTGAGCTCCG CCTCCTGTGA GATCAGCAGC AGCATTAGAT 720 TCTCACAGGA GCGTGAACCC TCCTGTGAAC CGCGCATGCG AGGGATCTAG GTTGCATGCT 780 CCTTATGAGA CTCCAGTGCC TGATGATCTG AGGTGGAACA GTTTCATCCT GAAACTACTC 840 CCTTCCCTAC CCCATCTATG GACAAACTGT CTTCCACGAA ACCAGTCTCT GGTGCCAAAA 900 AGATTGGGGA CCACTGTCAG AGAAGTACGT GTAAAGTCAT TAGGATAGGT TAAATCACTC 960 GGAACAGTGT CTGGTTTAGT AAGGCTTACC GCTGCTGCTA CTCCTCTGCC TACTTATTCT 1020 TCATCAAGTG ACCAGTTTTC AGCCGTGGTT 1050
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