Tag | Content |
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EnhancerAtlas ID | HS133-10410 |
Organism | Homo sapiens |
Tissue/cell | melanoma |
Coordinate | chr15:78495310-78497960 |
Target genes | Number: 10 | Name | Ensembl ID |
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TF binding sites/motifs | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
Gata1 | MA0035.3 | chr15:78496357-78496368 | AGAGATAAGGA | - | 6.02 | POU4F2 | MA0683.1 | chr15:78495337-78495353 | AAGAATATTTAATGAC | + | 6.3 |
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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 |
GH15I078203 | chr15 | 78495411 | 78500229 |
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Enhancer Sequence | CATGCAGCCA TTAAAATAAA GTACAAAAAG AATATTTAAT GACATATGGA AATGTTCACA 60 GTATAACATC AAGTGAAAAG GGGAGCAAAA AAGGGCATAC AGAAATGCAT AGACCACACT 120 GAAAAGATCT GTATCGAGAG ACTTAGGAAA TCAGGATGAC TGCCAGTCCT TAAAGTAGTC 180 CTCATCTCCC CTTTGTGCTC CACCAACAGG GCACAACCAT CAGCTCTGTC CCATGCCCAA 240 ACTAAGATCA GTGCAACCAT CAGCTCTGTC CCATGCCCAA ACTAAGATCA CTGCTGTAGT 300 AACAGCCAAG AACGGGGCCA GGACACAATC AAGGTCTCTG TTGCCCAGCA AGGCACCCAG 360 ATCCCAACAG GAGCTGACTC CAAAAGGCAA CCAACGACTA GATCTACAGC GCAGTGGAGA 420 ACCCAGAAAG CTCGCTGCCT GCTGCCAATG CAGCACCACC AGCACACTGC CCGCCCACCA 480 AGTGCCAAGT CAGCTGAGAG CTGGGGGGTA GGCTTTCCCA GGCAAGGTTG GCACTCTCTG 540 CCGCCTCCCT CTCCCTCTGC CGCTTCCTCC CTCTGCCACT TGTCTTGGCC TGACCCTGGC 600 TTGTATCTTA TCAATCCACC CTTTATGCTG GGGGCCACTG GGCAGGCAGG GAGCTGTGTT 660 CTCTGGGGTT CTGGAATAAA GGCGTCTAAA GAGCAAAGGC AGTCACTCAA TTAGCCGGGA 720 AGGAAAACAA CACAAGAGCA GAGAGCGGGA GGCTGGGGCT GTTTTCCGTG GTCTGTGGGA 780 AAGGCTGCAG GAAAGTAGCT TCTTGTGCAG ATGGAGGAAT AACTGGTGTT GAGGAAGAGG 840 TGGGTCTCAG GCCTAGGACA GATCTCTCTC CGAGAACGGT CCTGCAGGGC ACTGACCCCA 900 GAGGCCCTCC TCCAAAGGCC AGGCAGGAAC CAGCCCCAGG AGGGCCCCTC TCTCCAACAC 960 GGGACCCTGT GCTGAGGGCC AGCCCAATGC AAGGCACTCT CAGGGATACA GAAGAGGAAG 1020 AGGCCACATT GGCCCCAGGA CATGAAGAGA GATAAGGACA AGACCTAGCA CAGAAGGGTC 1080 TGTCAGCTGT TCAGTAGTTC CTCTGTGTCT GAGGGGAGAG GGCCCCTGCA GCTGCCACTC 1140 CCGGCCTTCT CAATGGGGAC TGAAGAGCTC TGAGTTCTGG CCACCACAGC AGAATGACCC 1200 TGGGCCTCAG TTTCCCCATC TGAATTACAA TTGGGGTAGA CAAGATGTTC TCTATACGCT 1260 TCTCCACAGT CATTGTTTTA GCTTTTTAAA ATTGCCTCTA GGATTCCACT TGTCCAGGCC 1320 TGGACCACCG GGGTAAGGGA CCTGAGATGG GCTTTACCTG CCCCTGTAAA GGTGAGCATG 1380 CTCAGGAGAT GTGCAGGAGA CCTCAGGCTG GGTCTCCATC CACTGGAGAG AAGCCGGGTC 1440 TGAGCAAGAA CCCGGGCATC CCAGCCAGAA GCCCTGGGCT GGCCTGCCCC AGACCTGCCC 1500 CACATGGCAG GGTCCTAGGA GGGGACACCC AGGCAGTGTC TGAGGCTGTC CAGGCAGGGG 1560 CTGGGTGGGT GCCTTGACCC CTGCGGAAAA TGTTTCTCTG AGGACCCCCA GAGGTTCCAC 1620 TCATTTTGGC TGGCAGGGCC GGGATTACCT GTTTCCATAT CATGGAGAAG GAATCACTGG 1680 CACTCATTTC CTCTGACCCT TGGAAAGCCT TTCCTGCCGG CCCCCATCGG AGGCTGCGGG 1740 GACAGGCAGG TCCTCTTGCC TTCCACTGTC CCAACGGCCT CCTCCTGCTA CCCGGCCTCA 1800 AACTGTGAGC TTCTTGAGGA CAAGCATTGT ATCAGGCCTC TTTCTGGCTC CCTAGCGCAT 1860 AGCTCCAGCC TGAAACACCA CCCCTTGCAA CATTTGGGAA GGGTGGGAGT GACGAACCGA 1920 GGGAGGCCCA GCAAATCCCT TGACCCACAA AGGGCTTCAC TGGACTGGAG ACAAGTGGGG 1980 CTGAGCACCT AGCTTCCCAA TTGCAAAAGC TCCTTAGTGG GTGTGGGAGT TTCCTAGGGA 2040 GAAAGCGGGT GGGGAGCCAG CCCTGGCCAG CACCTCCAGC AGTTTCATCC CCAGCAGCTG 2100 CTCACCCCGG GTGCCCTCCC CTCTCTGTGG TCTCGATGCT GCCCTTCTCC TGCTGGGCTT 2160 CAAGCTCTAT CTAGAAAGGC CTAGAAAGTA AAAAGTAATG TGTCTCCAGG GCCCAGTACA 2220 AGGCTGCCTT TGTGTGAAGG TCAGATTCCA GTGTCTCGGT GGCCTGACTT CGCACAGCTG 2280 CTTCCTGGGA GTACAGCCAT CTGGAGAGCT CAGAGCTCAG CCTGGGGACC AGAGCTCAGG 2340 ACCTCAAACT TTTTGGGACC TCAAAGAGAT CTGGGAGCCT CCGAGGGCTC CAGAGTGAAC 2400 CCTGATTCCT GTGTACAAGA CTCAAAGAGC TCCCCAGAGG GGCTGCCAGT GTCTGCAGTT 2460 AGATGAAAGG GAGGCAGGGG CTGGCCAGAC TTGTGGGGGC CAGACCTGGA AGACCAGACT 2520 GCATGATGCT ATCTAGGTCC CAAAGAGGCA GTGTGGCCAG TTAAGAGTTC CACCTCTTAC 2580 CAGCTGTGTG ACTCTGAGAA AATCACTAAC CCTCTCTGAG CTCCATTTCC TCTACCAAAT 2640 AGGAGTGATA 2650
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