Tag | Content |
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EnhancerAtlas ID | HS133-32372 |
Organism | Homo sapiens |
Tissue/cell | melanoma |
Coordinate | chr9:132268020-132269920 |
Target genes | Number: 21 | Name | Ensembl ID |
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TF binding sites/motifs | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
HES2 | MA0616.2 | chr9:132268361-132268371 | GGCACGTGCC | + | 6.02 | HES2 | MA0616.2 | chr9:132268361-132268371 | GGCACGTGCC | - | 6.02 | HSF1 | MA0486.2 | chr9:132269398-132269411 | TTCCAGAATGTTC | + | 6.54 |
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| Number of super-enhancer constituents: 5 | ID | Coordinate | Tissue/cell |
SE_34236 | chr9:132235634-132270098 | HCT-116 | SE_34620 | chr9:132269064-132270625 | HeLa | SE_38576 | chr9:132268889-132269805 | HUVEC | SE_55785 | chr9:132268758-132269939 | u87 | SE_67584 | chr9:132268758-132269939 | u87 |
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| Number: 1 | ID | Chromosome | Start | End |
GH09I129507 | chr9 | 132269279 | 132269679 |
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Enhancer Sequence | CTCTCCTGGA GGAGATGCTC CCCAAATTAG CCATCATGAG CGCTGGCTCT GGGGGTTGGG 60 CGTTGGGGAG CAGTTTGCTC AGCTGTAAAA TGGGAATAAC AGAAGCCGTC CCTGGGACTA 120 TGAGATCAAG GTGCTCAAGA AAAGTGGTGT CTGCTGAGGG GAAAAGCCAG TCCCAAAAGG 180 TTGCATACTC TCATTCTGTT TATTTGTTTT TGTTTTTGAG ACAGGGTCTC GCCCTGTCAC 240 CCAGGCTGGA GTACAGTGGC GCAATATGGG CTCACTGCAA CCTCCACCTC CTGGGCTCAA 300 GTGATCCTCC CATCTCAGAC CCTCAAGGAG CTGGGGCTAC AGGCACGTGC CACCGTGTCC 360 GGCTAATTTT TGTATTTTTT GTAGAGACAG GGTTTCACCA TGTTGCCCAG GCTGGTCTCA 420 AACTCCTGAG CTCAGGTGAT CCGCCTGCCT TGGCCTGCGA TAAAATTGCA CAGAAGTAAA 480 TACACACACG TGAGGATACG GAAAACCGGG GAAACCTGAG CAAGAGCAGT CAGACCCCGG 540 CTGTGATGGC GCCCAGTAGT TCTGCGAGAT GTTACCATTG GGGAAACTGA GTGAAGGCGG 600 GTACCTGGGA TCCCTCTGTT TTCTTTTTTG TTGTTGTTGT TATTTTGAGA TGAAGTTTCC 660 CTCTTGTTGC CCAGGCTGGG TGATCCACCT GCCTCGGCCT CCCAAAGTGC TGGGATTACA 720 CGCGTGAGCC ACTGTGCCCA GCCTCTCTGT TTTATTTCTT CTTTTTTTTT TTTTTTTTTT 780 GGAGACGCTC TGTCGCCCAG GCTGGAGTGC AGTGGCACGA TATTGGCTCA CTGCAAGCTC 840 CGCCTCCTGG GTTCACACCA TTCTCCTGCC TCAGCCTCCC GAGTAGCTGG GACTACAGGC 900 GCCCGCCACC TCGCCCGTCT AATTTTTTGT ATTTTTAGTA GAGGCGGGGC TTCACCGTGT 960 TAGCCAGGAT GGTCTCAATC TCCTGACCTC GTCATCCGCC CGTCTCGGCC TCCCATAGTG 1020 CTGGGATTAC AGGCATGAGC CACCACGCCC GGCTGTTTTA TTTCTTATAA CTGTACAGGA 1080 ATCTACAATG ATTGTAACAA AAATTTCAAT TAAGGCCACT CTAGGCACAT GGCCTGTGGG 1140 GTAGCCCTGC TCAACAAGAA GCCGTCAAAA AAATGTTTTT TAATTAAAAA ATTTCTTCAA 1200 TTAAAAAGCG TTATCTTCCT CTGCCCGGAA AGGGTTAAGT GAGTCACTGC AGTTAGCTCC 1260 CCTTCCCCCA CAACCACCTA GACCAGGCCA GGGACCAGCG GGCAATTGCC TGGCAGCTGG 1320 AGTTTTCCTC CACTGTGGAC TGTACTTCTT GCGTCACTCT GAATGTCTCC AGTCTTTATT 1380 CCAGAATGTT CTGGTCCTCT CCCACTTTTC CAAGGACAGG AATTCCCTAG TGGGGCTCCA 1440 GAAGAGGCTC TGGAGGAGAA CAAGAAAGGC CCTTGTCATC CATTGGCCTC AGGCTGGGAA 1500 ATCTCGGTTC CACTCCCAGC CCAGCCTCAA TATTAGGTTG TCAGTCTGGA GTCTGAGAGC 1560 CATGCCCCCA CCCCCTTAGT CCTTCACCTC CAGGAGAGTT GGGGATACTG GAAAGAATGT 1620 TGAGTGTCAG AGCCCCTCTC AGTGGCTCAC GCCTGAAATC CCAGCCCTTT GGGAGGCTGA 1680 GGCAGGTGGA TTGCTTGAGG CCAAGAGTTC AAGACCAGCC TGGCCAACGC GACGAAACCC 1740 TGACTCTACT AAAAATACAA AAATTAGCTG GGCGTGGTGG CACACACCTG TAATCCCAGC 1800 AGCTCGGGAG GCTGAGGCAG GAGAATTGTT TGAACCTGAG AGGTGGAGGT TGCAGTGAGC 1860 TGAGATCACA ACACTGCACT CAAAAAGTAG TTAATTAATT 1900
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