Tag | Content |
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EnhancerAtlas ID | HS133-14202 |
Organism | Homo sapiens |
Tissue/cell | melanoma |
Coordinate | chr18:43732280-43733720 |
Target genes | |
TF binding sites/motifs | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
ZNF263 | MA0528.1 | chr18:43733576-43733597 | GGATGAAGGAGAGGAGAGGAA | + | 6.07 |
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| Number of super-enhancer constituents: 1 | ID | Coordinate | Tissue/cell |
SE_59275 | chr18:43731525-43756409 | Ly3 |
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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 |
GH18I046151 | chr18 | 43731850 | 43734097 |
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Enhancer Sequence | AGATGATTTG TGGGCAACAC AGAAAGCCAG TACATTAGGG AAGTCTCTTA ACCTCCCTGG 60 GTCCCAGTTG TGCATCTGTA AATTAGGGAA ATGGTTGAAC CGGGTCACAC CTAGGAGCCT 120 CTCAGGCTCT AGCTTTTGGA GACTCTGTAT GGGCAGATGC TGAGTGCTGC ACCGTTGTGA 180 GAAGGAAGAA TCGTTCTCTA ATGGGTGAGC AGGCTAGTGC TCTCATGTGG GGGGCTGTGG 240 GTGCCAAGGA GGTGTGTCGT TGAGGTGGCT GCTGCAAAAT GCAGACAGCT GAGGACTCAC 300 CCTGAGTCCT TGATGACCCA TCTGCCAGCA GGCTAGACGC TGACCACAAC TGGCACCACG 360 CCTGGCTGCA GAGGCGATCA GCTTTCAAGA GCAGGAAAAA CAAATGTCCT CTTTCCCCTG 420 CTCTGTAAGG GACGTGCAAC CATGCTGGGC ATCCATCCCC ACCTCTGTTA ATTTACTGGG 480 GGGCAAAGGG TCCACTCTGC AATCTTCCTC CCATGATACC TAAAACTCTT GGGCTTGTGA 540 CCTCTAGGAC TGCCCTGGGG AGCTCCTGGG AAGCTGAGTC AGGGAGGGCA TCAGGTTTCC 600 TGCTAGCTCT TGGCACACTT CTGAAGTAGG TGAGCTTGTG CTTCTGTGCT GTCCCACCCA 660 GCCGGTCTGC CAGGTCTCTC TGCTTCCCAC ACCCGCTGCC GCCTGCCCCA GGGGCCCGGA 720 CCACCAACAC ACCCCAGAGG TGGGGCACCC ACTGTCTGCC TTCCCTCCCC CAATACTCCC 780 TCACACACAG CTGACACGCT CATCTGACTG GCTAAAGGGA TTGTCCCTTA TTAAATTCCT 840 TGGGGGATGA TCTCATTAAG CCTTGTTATG GGTCACTTCT ATTTCAGGGA GAATAAATTT 900 GCTGCAATCT ATGGGCAGCT AGTTAATTGA AACCTGAGGA AGGGGCTGGG GGAGGGGAGG 960 GCACGGGTGA GGGGGTGGAG CGAGCCTGAA AGTGTGGGAA GTGCCTGGCC TGGTGAGAGC 1020 TGAGAGCTGG CTGGGAGGAG GCTGAAGGTG CACATGAGGG TAGCCGATAA GGAGGAGGCC 1080 ACAGGCAGTG GAGGGAGAGG GGAGACAAAA GCAGGTGTCA GCTGCAGCCT GATGCAGGGA 1140 GATAGCCTCC TAACTGCCTC CCAGGCCTCT GTGCTCAGCC CTGCCCCAAC ATATGAGTCC 1200 AGGCCAGCAC AAAGTGATAA GCACCTAGGC CAGGATGTAG CAACAGAGAT GGAAAAGAAG 1260 GAGATATGAG AGAACTTGGA AACAAATTTG ATACAGGGAT GAAGGAGAGG AGAGGAAAAA 1320 ACCCAAGATG ACCTTTAAAG ATGCTTGGAG AATGGGGAGA GGCGCCAGCC GGAGCACAAG 1380 CCCAACACAG GCCTCTGAGC AATGCCAAGT TTACTGCTCT GCTGTTTAAA GAATCCTTCT 1440
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