Tag | Content |
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EnhancerAtlas ID | HS133-31749 |
Organism | Homo sapiens |
Tissue/cell | melanoma |
Coordinate | chr9:73218390-73220060 |
Target genes | |
TF binding sites/motifs | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
HES2 | MA0616.2 | chr9:73219704-73219714 | GGCACGTGCC | + | 6.02 | HES2 | MA0616.2 | chr9:73219704-73219714 | GGCACGTGCC | - | 6.02 |
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| Number of super-enhancer constituents: 1 | ID | Coordinate | Tissue/cell |
SE_45679 | chr9:73214224-73219117 | Osteoblasts |
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| Number: 1 | ID | Chromosome | Start | End |
GH09I070604 | chr9 | 73219456 | 73219798 |
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Enhancer Sequence | AAGGAGACAC AATACAGTGC TCTGGCTGTT CAGGCCCAGG AGCCCCAGCA TCAGCCAAGG 60 CCACTGCACA GCAGCACAGA GCAGGGTCAG CAAGCAGGAC ACAGACTTTA TGACAAAAGG 120 AACTTGAAGG TGCTAAACTA ACAAAAGAAT TAGAAAAGAC AGTAATACTT GAAGGATTAT 180 AATATGCAAT CTTCCTTTTG ACCTGTACAT GTATCTCTGG GGCTCTGGTG CTTCGTTTAA 240 ATCTATGTGT CATGATGCAT CATTTCGCCT TGCAGTTACC CATTTTTGTG TGTTTTCTTG 300 GCTAAAAAGG GAGCCTTGGC TGTCAGTGGC GGCTCTTGCT CAGGCGTGGA CCTTAGGTTC 360 TTAAACTAGG GCAGCACAGT GGATTTTTGC CTCACGAATG CCAGGCAGAA TAAGTGTCTG 420 TGAGAAGCAA AGGAAGAGGA AGACACATGT AACACCTGTA AATTGGTCAA ACCAACATAA 480 AAATAGCCCA GGCTTAAAGT GCTTCGCTTG TCAGTGCCCT GGGAGGGTCT TACCTGTTTT 540 CATTTCACCA CTTTCCTGTC CTAATCAAGT TAAGATAAGA TATTCCTTCC TGGTGTCTGC 600 TTCATTGAAA CAACACAAGA AAAGACAACA CAGTTTACAG AAAGGAAAGG GTCCGTGTGG 660 CCTTTTGTGG ACGGGTGTGG GGTTTAATCC CCAAGAGGCT CTGGCTCGTG GGGTTGAATC 720 CTGATGTGAC TGGCTGAATT GCTGGATGTC TGGGAAGAAC TCCCTAGGGT TTGGTGACTG 780 CTCCTGGAAG ATTCAGTTGT GTCAAGGTGA GTGAAGTGCA GGGAAACTGG TGGCTCTTGC 840 ATAAGGGGCT GAGGAGCCTT GAGAGAAGAC TCACTCACCT TAAGGGAAAT GGCAGACTAG 900 CTGGGCCTTC CTTACACAAT GCCTCAAGTC AAGTGAGGTA CTCACTGGCC TTAGGGGCCT 960 CAGGGGCTGT GAGCAGGAAC CAAGAGGGAG TTTATTAACT AAAATCTGCT GCACTCTTCA 1020 GAGTGGTGTA GCAAAGAATA GACACAGTGT GGGTGAAAGG ATTGAGGCCT TGAGGGGTCT 1080 GGAGGTACTG CATGACTTTG TAGCTGGGAA GGCAGCTTAG AAGGTGGAGG AAGCTGCAGC 1140 CTTGCTGGGG GATATGCTGC TTTCTCTACT AATTCTCTTA TGTTTTGGGA CAGGGTCTCA 1200 CTCTCGTCAC CCAGGCTGGA GTGCAGTGGC ATTGTGATCT CGGCTCATTG TAGCATTGAC 1260 TTCCTGGGCT CAGGTAATTC TCCTACTTCA GCCTCCTGGG TAGCTGGGAT AACAGGCACG 1320 TGCCACCACA CCCAGCTAAG TTTTTGTATT TTTAGTGGAG ACAGCATCTC ACTTTGTTGG 1380 CCAGGCTGAT CTCAAACTCC TGGGCTCAAG AGATCCTCCT ATCTATCTTG GCCTCCCAAA 1440 ATGCTGGGAT TATAGGCATG AGCCACCATG CTCAGCTGAA TGGATTCTTC TTTTTTTTTG 1500 GAGACTGAGT CTCACTCTAT TGCCCAGGCT GGAGTGCAGT GGTGCGATCT CGGCTTTCTG 1560 CAAACCTCTT CCTGGGTTCA AGCGATTCTC GTGCCTCAGC CTCCGGAGTA GCTGGGATTA 1620 CAGGCACCCA TTACCACGTC TGGCTAATTT TTGTATTTTT AGTAGAGACT 1670
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