Tag | Content |
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EnhancerAtlas ID | HS133-20293 |
Organism | Homo sapiens |
Tissue/cell | melanoma |
Coordinate | chr20:62799690-62800900 |
Target genes | Number: 25 | Name | Ensembl ID |
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TF binding sites/motifs | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
NEUROD2 | MA0668.1 | chr20:62800240-62800250 | ACCATATGGC | - | 6.02 | TBX20 | MA0689.1 | chr20:62800301-62800312 | CTTCACACCTC | - | 6.02 | ZNF263 | MA0528.1 | chr20:62800402-62800423 | AGAGGAGGAGCGTGAGAAGAG | + | 6.1 | ZNF263 | MA0528.1 | chr20:62800405-62800426 | GGAGGAGCGTGAGAAGAGGGG | + | 6.69 |
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| Number of super-enhancer constituents: 1 | ID | Coordinate | Tissue/cell |
SE_65388 | chr20:62797093-62801872 | Pancreatic_islets |
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| Number: 1 | ID | Chromosome | Start | End |
GH20I064165 | chr20 | 62797094 | 62801872 |
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Enhancer Sequence | TTCTCCCCAG GGTTAATGCC ATTAGGAGCG TTCCTTGTGG GAAGATTGGT TTCACCCATC 60 ACTTCATCCT TTTTTTTATT TTACAATTTG CACTTAAAAA TGCAATGTTA TTTTAATCGG 120 GAACGAAAGT AACTCAGCGT GCTTTAATCT GCCCTGGCTG AGTACATCTG CCTTGGCCAG 180 GATTGGAGTC CAGGCCTTGC AGAGGAGAGA GGATGTCGAC ACAGCTGTGG GTGTCTGTGG 240 TCCTCCTGCC ACCCCTTGTC CTGCAGCACC GGAAGCCTCC ACTCAGCAGC CCCAACCTTC 300 AAGAGAGTGA CTTTGTGCTC TGGCAACTGA GTGTGTGGTT TGCCCTGGGG TTGCTTGGAG 360 TTGATTGGAT ATGTTCCCTG TGCCTTGGGG TTTATTTGGG ACTGTGGCCT GGGAGCACGG 420 CCTGTGCCAG GAGGGTGCAG GTTGGATGGT CCTCAGGAAG TAGGCTGCAG CGCTCTGCAG 480 GAGTCAGGGT GGCCAGGCAA GGTGGGGGTG AGCACTGGGG ATCTGGATGC TCGGGAGGAA 540 AGGTGGAGGC ACCATATGGC CTGAGCTGCT GACAGATGAG CCTGCTGGCC CCACCTCTCT 600 CTCACGCCTG GCTTCACACC TCCATCGTGT TCAACACTGG TCTGAGGGCT GGGGCAGAAG 660 CCATCTGGGT CCTCTTCTTT TTTTCCATTT TGCTGCCTGC AATCCACACA TCAGAGGAGG 720 AGCGTGAGAA GAGGGGGCCC TGGGTCAAGG CGGTTGGAGC CTCTCACCTG GTCCTGGGGG 780 ACCCTCCATG TCTCCCTCAG GGACCCACAG AGCTGCCAGT GGCTGACCTG TCCTGCCTGA 840 GTGGGAGGAG AGTGGGAGTT TGGATGCTCC ATGGTGCACC AAGGCCTGCT TTAGAAGGCC 900 CTAGAAGGTC CCTGAGACTC TCGGACCGCA AACTGACAGC AGCAGGTGCC TGGGGTGGCC 960 TCCCAGTGAG CCAGAGCCAC AGACCCGAGG CGCGTCCCCA ATCCCGGTGT GCGCCTCGCT 1020 GAGCTAGCTT GTCAAAGCGC TTGGGTCTTT ACACCTACAG GGTTTTTGGG TTCTGAAAAT 1080 CAAATGGCTT TAGCAGTCCT GCTCTGTGGG CAGCCAAAGT GGCTCCTAAC TGAAGGTGCT 1140 GCCCATTCTT TACAAGACTT AGAGCTGGGG GACAAGTTCC CTCTTGGCTC TGAGTTTCCC 1200 AGGATAACTG 1210
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