Tag | Content |
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EnhancerAtlas ID | HS133-16083 |
Organism | Homo sapiens |
Tissue/cell | melanoma |
Coordinate | chr19:51866740-51868320 |
TF binding sites/motifs | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
ZNF263 | MA0528.1 | chr19:51867480-51867501 | GGAGAAGGGAAAGAGGGTGGG | + | 6.06 |
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| Number of super-enhancer constituents: 1 | ID | Coordinate | Tissue/cell |
SE_24259 | chr19:51866988-51867461 | Colon_Crypt_2 |
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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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Enhancer Sequence | CACCCAGGCT GGAGTACAGG GACACAATCC TGGCTCACTG CAACCTCTGC CTCCCAGGTT 60 CAAGCGATTC TCCTGCCTCA GCCTCCCGAG TAGCTGGGAC TACAGATACG TGCCACCATG 120 CCTGGCTAAT TTTTTTATTT TTAGGAGAGA TGGGGTTTCA CCATGTTGGC CTGGCTGGTC 180 TCAAACTCCT GACCTCAACT GATCCACTCG CCTCAGCCTC ACAAAGTGCA GGGATTAGAG 240 GTGTGAGCCA CCGCGCCTGG CCGAGAATCA CTAGATTTTG ATATAATCCA TGAGTTGGAG 300 TTGGGCAGGA CAAAGGACAG AAAGCAGAGG TAGGAGGGTG GTGCTGGAAG AAGGCATGGA 360 ACGGGCAAGC CGCGGCCTGG TCTGTCAGGA CAGGAGGAGC AGGTCACAGT GGCAGAAGCA 420 CAAAGGGTAA GGGAGGGTCC AAGGAGGGAA GTGGACGGCT GAAGCAGACC ATGAAGAGGA 480 GGCTGGACCA CAAAGCATCC CAAATGCCAG GCAGAGGGGC TGCGACTCTG TCCTGAGGGT 540 GCTGGGGAGC CACAGGCAGG CTGGGAGCAG GGGAGAGCAG GGTGAGCTCT GGGTGCAGAA 600 AGGCCCCTAA GGCTGGGTAG AGGTGGGCTG AGAGGGAGAG ACTGGGAGTG AGGGAGGACC 660 CGGGTGAGGG TCCAGGTGAG ACAATGACAC CAAGAGACAA TAGGGCAAGA AGGGTGGGGG 720 GTGGAGAACT GACAGCTTTG GGAGAAGGGA AAGAGGGTGG GACAGTACCC AGGTCTAATC 780 TGGTGTTTAG GAAGCTGGCA GGGTCTGAAT CATTTATTTG TTCTGAAAAG GACATCAACA 840 GACACATCCA GTGAGACAGG ATGTAATGCA GGGAGCCCTG GGGCACTGCG GGAGGGGAAG 900 GCAGCACCCT CTGGAAAGGA CAGTAGCTGA TTCAACGCGG CCTTCACGCT TCCCCTCTGT 960 TCTCTCCCTG AGCACACCAG AGACATCCAT GTGCCAGGCT CTGTGCTGAG TGATGCTGGG 1020 ACCAGAGCTG AGTCAAACGT GGGCCTGCAC CATGGGGGAG ACGGATCCAA TCCCAGACAT 1080 GCCAGGCGTG GAAGGCCAGG GCTGGGATGG AGAGAAGAGG CCCAGGGAGC TGTAGGACTC 1140 CAAAGATGTG ACAGTAACGA ACAGTCAGAG CAGGGAGGAA ACCAAGTGTT GGGTCCCAGG 1200 ACCCCAAGAG GAATGTGTCT CAAAAGGGCT ACAGGTGACA TCCCTGTCAT GTGCTGCCAG 1260 AGGCATCATT AGGACAGGGG GCATTGAGGG AGATGGGAGA GCAGAGTCTA GAGCCAGACT 1320 TGCCCGGGGT TTCGATCGTA ACTCTGCCAC TTACTGGCTG GGAGATCTGA CAGGCCTCAG 1380 TTTCCTCATC TATCCAATGG AATTAATAAT ACAAAGGGTC GGCCAGGCAC GGTGGCTCAC 1440 ACCTGTAATC CCAGCACTTT GGGGGGCCGA GGCAGGCGGG TGGATCACCT GAGGTCTGGA 1500 GTTTGAGACC AGCCTGACCA ACATGGTGAA ACCCCATCTC TACTAAAAAT ACAAAAAATT 1560 AGCCAGGTGT GGTGGCACAT 1580
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