Tag | Content |
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EnhancerAtlas ID | HS133-11074 |
Organism | Homo sapiens |
Tissue/cell | melanoma |
Coordinate | chr16:19016520-19018490 |
Target genes | |
TF binding sites/motifs | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
MEF2B | MA0660.1 | chr16:19017024-19017036 | GCTAATAATAGC | + | 6.07 |
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| Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder | Number of disease enhancers: 3 | Chromosome | Start | End |
chr16 | 19016606 | 19017680 | chr16 | 19017780 | 19017800 | chr16 | 19017800 | 19017874 |
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| Number: 1 | ID | Chromosome | Start | End |
GH16I019005 | chr16 | 19016524 | 19018195 |
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Enhancer Sequence | CTGCTTCAGC CTCCCAAGTT AGCTGGGACT ACAGGCACCC GCCACCATGC CCGGCTATTT 60 TTTTGTATTT TTAGTAGAGA TGGGGTTTCA CCATGTTAGC AGGATGGTCT TGATCTCCTG 120 ACCTCGTGAT CCACTCGCCT CGGCCTCCCA AAGTGCTGGG ATTACAGGCG TGAGCCACCA 180 CGCCTGGCCC GCATGTTAAA TACTTTAAAT GGCCTGGTAC AAGGTAGGCA AGTACTCAAT 240 AAATCTTAGC CAGTGTTGTT CATGTTGTTT GCAACTCCTT CCTCACCATC ATGCTGATGA 300 GGCCCATGGT ATTAGATCCT CCATTCCCGA GATGAGAAAA ATGTGACTCT GAGGCAGCTG 360 TGGTCTCTCC TGGGGTGGCT TGGCTGGTGG GTGACAGGCC AGTATTTTAA ACCAACCCAG 420 GCTCCAGCCT GGGGCCCCTG ACCCCACAGC TGTTGAATAT TCAGTAGGTC CATGCTGTTC 480 TATATTCAAA GACCTTTGTT TGTGGCTAAT AATAGCTCTT TGTTTCTGCT TGCAGGAGGG 540 TAGCCTCCAT GCAGGGCTTA GACCCTTTTC CTTTTCAGGG ACCACACCCA CCCTACCCTC 600 ATATTGGCTC TAGGGAGCCA CTGCCACTAA TGGAAGTGTG TCATATCCTC AGGGTGTGCC 660 AGGCAGGGAG GTAGAAGGGT GGGTGAGGCT CGTAGACTTG CACATGGTGA TTGGCAGGGC 720 CCCAGCCACG TGTCCATGTG TCATCTACAG TGGGACAGCT GCTCCATTGT GTCTGAACTT 780 GCCTATCCGA GAAAGGCAAA GATTACAGTG TCAGAGCCAG GCCTTGACCG GTCCCCACCT 840 GGCCCTGCCC CTGCCCATCC TCATCCGGTT GGTGCCTTTA TGGAGCTCTG TGTGTGCCGA 900 GCACTGCCTG GGACCTTCTA CCCATGTGAT CCCCTTTAAT GTTCATAAAC AGGCTGTGTA 960 GCAAGTCCTG ACCCCAGCCT TGCCCTTGCA GCCTCCAGGG TGACCTTTTT TTTTTTTTTT 1020 GGACGGAGTT TCGCTCTTGT TGCCCAGGCT GGAGTGCAAT GGCACGATCT CGGCTCACTG 1080 CAACCTCCGC CTCCTGGGTT CAAGCGATCC TAAATAGCTG GGATTACAGG CACGCGCTAG 1140 CGTGCCCAGC TAATTTTGTA TTTTTAGTAG AGACAGCGTT TCTCCATGTT GGTCAGGCTG 1200 GTCTTGGACT CCCAACCTCA GGTGATCCCC TTGCCTTGGC CTCCCAAAGT GCTGGAATTA 1260 CAGGCGTGAG CCACCGTGCC CGGCCCAGGG TGACCTTTTA AAATGCAGTC AAAGCACAAC 1320 ATCCCAAGGT CCTGCCACAG TCTACAAAGC CTGACTTGGT TCGACCCCAG CCACCCCTCT 1380 GACTTTAACG TTTCCATTCT CCCTGTCCTA AATACCTATT GTTGCTCAAC ACACTGCTCC 1440 AAATGTGCTG GCTTAAGCCA TGTTGTTATT TCTGCTGATT CTGTGCATCA GGGACGATGC 1500 AGGGCACGGG GGAGCCCGCT TGCACTGCTG CCTGGGATGT CTGCTGGCGC TGGAGCACCC 1560 AAGATGGCCT CATCATGGCG ATGCCTGGTG AGGATGCCCC AGGGGTTTTT TTTGTTTTCT 1620 TTTGTTTTGC TTTTTTGAGA CAAAGTCTTG CTCTGTCGCT TAGGCTGGAG TGTAGTGGTC 1680 CAATTTCGGC TCACTGCAAC CTCTGCCTCC CAGGTTCAAG CTATTCTTCT ACCTCAGCCT 1740 CCTGAGTAGC TGGGATTATA GGCGCGTGCC ACCACGTGCA GCTAGTTTTT TTTTTTTTGT 1800 ATTTTTAGTA GAGATGGGAT TTCACCATGT TGGCCAGGCT GGTCTTGAAC TCCCCACCTC 1860 AGGTGATCCG CCTGCCTCGG CCTCCCAAAA TGCTGGGATT ACAGGTGTGA GCCACCGTGC 1920 CTGGCTGTCC CAGGGGTTTG AAGACACGAG CCTGGGGCCT TGGTTCTTGC 1970
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