Tag | Content |
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EnhancerAtlas ID | HS133-05087 |
Organism | Homo sapiens |
Tissue/cell | melanoma |
Coordinate | chr10:129862100-129863780 |
Target genes | |
TF binding sites/motifs | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
ZNF263 | MA0528.1 | chr10:129863160-129863181 | GAGGGAGGCAGAGGGAGGGGG | + | 6.68 |
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| Number of super-enhancer constituents: 7 | ID | Coordinate | Tissue/cell |
SE_09432 | chr10:129855455-129865319 | CD14 | SE_16628 | chr10:129860104-129864114 | CD4_Naive_Primary_8pool | SE_18605 | chr10:129859223-129865362 | CD4p_CD25-_Il17-_PMAstim_Th | SE_19348 | chr10:129859867-129864390 | CD4p_CD25-_Il17p_PMAstim_Th17 | SE_20225 | chr10:129859801-129864659 | CD56 | SE_22673 | chr10:129859141-129864869 | CD8_primiary | SE_53695 | chr10:129859999-129864364 | Spleen |
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| Number: 1 | ID | Chromosome | Start | End |
GH10I128061 | chr10 | 129860027 | 129864802 |
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Enhancer Sequence | CGGGGGTGGG GTTGAGTGAC AGGCAGGGAG CCATGCCATA GGCAGTGAGC TCACTCTCCA 60 GAATGAAAGA AGAACTGGGA GCCTGAGGGA CACTTACCAC AGGTGGGGCG AAGTTAGGAG 120 GCTGTGCTTC TGGCGTGTTC TGGCATGAAG GCCCGGTTCA GTGGGAGCCG TGTGTCCTGC 180 CCGGCCCTGC TCAGGGCCTG CTGTGTCCTG AGCTCCTCAG TCATCTGCTG GCCTGGCCCC 240 AGCAGTTCCC AGGCATTGTA GCGAGGACTG TGGGGAAGGG CTGCCATTTT TAGATGGGAG 300 TACCAGGCCT TGGGGAGCTC AGCTGGGGCA GAAGATGGGT GGCAGGAGCC CACAGGAAGG 360 GCAGGCTGGG AGGTGCTCTG GTCCCCGCAG TGCCAGCTTA CTAATTGCCA CCCAAAACAC 420 AGGAAGCAGC CTCCAGCCAC CGTTTCTGGT CAGGAATAGG ATGGAGGCTT TCATTCTGCT 480 CTGGGGGGAG CTGAAACAGG ACTGTGGAGG GCCACCCCTT TGCCCTTGCA AATCTTGCCC 540 TTGTCATGCT TTGTCATGGG GAAGAGGGAA GAGTGACAGA GGGAAGTAGG GGATTCCCAG 600 CCCAGGACTC TTCACTCTGC CTGCGCTGTA GCGGCCATGG AGGAGGACAC CCACGCGAGG 660 GAAAAGGAGG CTGACCCTTC ATCAGGAGCC TCAGGGTCCC CCGTGACCCA TGGCCCATAG 720 GGACCAGTCT TCCTGGGGTT GGTGCTCCAA GCATGAGACC AGCACAGAAG CAGTGGGGCT 780 CAAGGACGCC CTCACTTCCC TCTTTCAGTC ATTCTGCTGA AAGTGTCACT GGCATTTTCT 840 CTCCATCTTC CCCCACAACC TCCTACTGGA TTTTTCCACT CCTGTGACTC AGTGCTGGGC 900 TGCTGCCGCG TCCTCATTCT CACCAATTCA GATGAAATCA TTTCTCAATA GAGTTCCCTT 960 TTTCTTAATT GCTCACACTT CTGTTGTGGT TTCCTTGGCT TCCACATCCT GGGCTCTGCA 1020 TTGCAAAACA CAGCTGCCCT GGCATCTCAT GATCGGGTGG GAGGGAGGCA GAGGGAGGGG 1080 GTATAAAACC AGCCACCAAC ACTGAGCCCT TGAGAGGCTG ACACATGTTC TCAGTTCCTA 1140 CTGGAGAGCC TTCAAGGTGA GAAGCTCAGG AGGGACCCCA GGGCTCCCCA TAGGGCCAAG 1200 ACTCACCCAA ACCGGGACAT GTAGGCATTT GCAATTCCCC TGGGCTGCAT CAGAGATGGC 1260 CTGTGACCCA CAGCCCCGCA GCCCCGCCCG GAGCCAGGTG TAAGGAGGGG GAAGTTGTCG 1320 GTAGCCGTCA TAACACAATG ATGCTGCTCT CTACTAAATA CCAGATGCTG TTTGTTTCAT 1380 AAGACTGTTA ATCCTGGAGG CTTGACCACG AGCTGTGCTG CTCAGGGGCC ATTCCCTGGA 1440 TATACTCTCT GACTACTGGC AGGCTTGTTC CATTCCAGAC ATGTTTCTCT GGCAGATGAA 1500 GTAGATCTTT TCCCCCTTGA GGTGGGTCCT CATTCACTCG CGAAGTGATG GAGGACACCA 1560 CCGGGCAGGT GCTGCGGGCG GTGCTGCAAA ATGAAAGGGC TCCTGGAACG TGTATTTTGG 1620 GTCATTCTTG CTTCAGAGGT CGGGAAGGTA AAGAAATGGG CCTGTCTGTA GCAATGCACC 1680
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