Tag | Content |
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EnhancerAtlas ID | HS133-12671 |
Organism | Homo sapiens |
Tissue/cell | melanoma |
Coordinate | chr17:41655120-41657690 |
TF binding sites/motifs | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
MEOX2 | MA0706.1 | chr17:41657578-41657588 | AGTAATTAAC | + | 6.02 | REL | MA0101.1 | chr17:41656315-41656325 | GGAAATCCCC | - | 6.02 |
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| Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder | Number of disease enhancers: 2 | Chromosome | Start | End |
chr17 | 41655519 | 41657569 | chr17 | 41657407 | 41657423 |
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| Number: 1 | ID | Chromosome | Start | End |
GH17I043577 | chr17 | 41654763 | 41657870 |
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Enhancer Sequence | ACTCCTTGCC TCCTGCCACT TCACCCCCTC CCCATTGCAG CTTCCCACGA GTTCCTTTCC 60 AGAGCCGTCG CTTGCTGAAT GGGTTGCTAG TGGAAATGTG GTTTTCAAAT TTGGGAAATC 120 TCCATTAAGT CCTTTTATTT AAGGAGGATG TCATTATCGC GCCTCCCTGA GGACTATTAC 180 GGTTCTATTA GGCAAGGCCG CAGACTTCCT AGGTACTGTC TGGGGTCTGA TTCCTGGGCA 240 GGAAAATGCA AGACAGGAAG AAGGGGAGGG GGGTTCAGAG AGAGAACAGA GGCTGGGGAG 300 GGGAAGCAGA AAGAAGAAAG GAGGAGAAAG AATGAAAGAG AATGCGGGAG GGAAAGAGAA 360 AGGAGTGAGG AAGTGACAGA GGGAGAGGCA AAGAGCCCCT CACCCCCCAG GCAGAGGAGA 420 GAGGGCAGAG GAGACCCTGG GCCACTTGGC CATCCGACAG TCTAGAGGAT TTACAATGAA 480 ACTGGACGCG AGCTGCCCGG AACTGGCTTC TCTCTTTCAT TAGAGACAGG GGATCCTGGG 540 GAGTTCTTCA TGCCTTCCGG CTGCCAGCCC ACCTTGGGGC CTCCACGTTC AGATTTGGGA 600 GAGGCCTCAG TGAGGGCTGG GAGGGAGGAA GAGGATGCCC AGGGAGGGTG GTTCTGGAAA 660 CTAGGTCTGA GCTCAGTTGG CCCAGAAGGG TGTTGGCCTG CCTGACCACT CTGGTGAACA 720 TAATGTTTTC CCATTCTCTG CTGCCCCCTC TAGAAGGCAA GCTCCAGAAA AGCAGACCTT 780 CTCTCTGTTC TGTGTTCTCT CTGCTCCCAG TCACTAGAAC AGTGCCAGAC GCATAGTAGG 840 TGTTCCATAA GTGTTTGTGG AGAGAATAGT AAATAATAGA AGTGGAAACA ATTCCACTGC 900 TTCCCCATCC TCTCCCTTGC TGCATTCAGA GCAAAGGTGG ATGGACCTCC TCTCTGTTCT 960 CAGTAAAGGC TTGTGACCCT TTACACACAC ACACACACAC ACACACACAC CCGGGCAGGA 1020 GGGTCAGGAA TCGCATGGCA AGCAGCTGAC ACTGGCTTGG CCAAATGAGA AAGGAAAATA 1080 TATATGCCCC TCCTGGGACC TTCTTGTTAG GGGGTTACCA TCTGCGGGCT GCCTGCTGGA 1140 AGTGCTTTAG CCTCTGGGCA GGAAGGCTGA TGTTCTGCGA CAAACATCCT GGCTGGGAAA 1200 TCCCCTGGCC CGTAGGTCCC TAGGGCCTGG GCAGCCTCCT TCCACGCCAT CCTGCCCTCT 1260 TCAGACCTTC CCCTGGCTCC TGGGCCTGAA GCCGGGCCAC CTCTCTCTGC CTCTGAGGGG 1320 CTCCCCCGTG AGAGCTAGCC CAGTGCCCCT GGGGCGTCCC CTCCCTCGGA GCTCCTGTGC 1380 TGAAGTGATT AATGAGGCAG GGACAAAGCC TTTCTTACCA GCTGTGTCAA CATGCCCCTT 1440 ACCCCGCGGC CCTGCTAGCT ACAGGTATGG GGAAGCAGCC CCCCACCCCC ACACCACTGC 1500 CCTAGGCAAT TGCCTCCTCC AAGCCTGTTT GCCCCTTACC TGGGCTCTCT TCAGGGTCCC 1560 AGGCCTCCCA CTGGGCCATC AGTGTCTGAT GGTGATGATG ATGATGATGA TTTTATGATG 1620 CTTACAGCAC TTGATGTTTG CTGAGAGCAT GACTCTCCTT TTTCTCAGCT CCTCTTTCCA 1680 GCTGCCTGAG CCAGGGGATC AGGTGTGGCT GTCTTTGGGT GACGGGGAGC AACTGGGCTA 1740 CAGTTGCTGG GACTGATACT GCCTCCTCTG TGAAGCCTTC CCTGATCACC TCTAGCAGGC 1800 TTTGTGTCTA TCCCTCTCCT CCCGTCCCTT TGTGTGTGGA GCTCGTCTGT TCCCCTCACT 1860 GCTTCCTTAA GGGAGGAGAT TCCTTCTCTG GGTATGCATC TTTGTACCTC ATCCCTCTTT 1920 CCCCACACCT CCATTCTCAA GACAGCCTAG CACGGTGCTT GGCGCGTGCT ATGTGCTATG 1980 ATAAATACTT ATGGAATGAA CCAATGACTT GTAGATCTGG AATGATCTGG AATTCCATGG 2040 CGTAGGTCTG TGTTGTCTGT GGTTCTGCAG ACTGATTACC TTGTGTTTGA TCTGTCTCAG 2100 ACCTGCCCAG GACCACACAT CCTGCCTCTG GCCCCAGCTG GTCTTTGTGG GGTTTCTAGT 2160 GGTTGCTGCC CAAGGAACTC TGTTGGGGAG GACGGTGACC TTGTGCTGGG GAGGACGATG 2220 ACCTTGTGCT GGGGAGTGGT GAGGGTGCGG TGGGGATTCA GAAAGCTGGA AGCAGCCACA 2280 TGCTTTTTTT TTTTTTTTTA ATGAACATTA CATTTTAGAA TAATGTTAGA CCTATAGAAA 2340 AGCTGCAATG ATAGCACATA GTTCTCATAT ACCCTTTACC CAGTTTCCCC TCATGGTAAC 2400 ATATTATGTA ACTCTGGTAC TTTTGTCAAA ACTGAGAAAT TAACGTTGGT ACATTACTAG 2460 TAATTAACTC CAGTCTTCAT TTGGATTCCA CCAGTTTTTC CATTAATATC TTCATTCTGT 2520 TCCAGGATCT AATCCTGGAT ACAGCATTGT ATTTAGCCTG CATGATTTTG 2570
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