Tag | Content |
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EnhancerAtlas ID | HS133-28729 |
Organism | Homo sapiens |
Tissue/cell | melanoma |
Coordinate | chr7:73251920-73253320 |
Target genes | Number: 16 | Name | Ensembl ID |
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TF binding sites/motifs | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
HES2 | MA0616.2 | chr7:73252035-73252045 | GGCACGTGCC | + | 6.02 | HES2 | MA0616.2 | chr7:73252035-73252045 | GGCACGTGCC | - | 6.02 | Nr2f6(var.2) | MA0728.1 | chr7:73252110-73252125 | CGAACTTTTGACCTC | - | 6.4 | RARA | MA0729.1 | chr7:73252107-73252125 | TCTCGAACTTTTGACCTC | - | 6.38 | ZNF263 | MA0528.1 | chr7:73252851-73252872 | GGAGGAGGGGGTAAGGAGAAG | + | 6.34 |
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| Number of super-enhancer constituents: 2 | ID | Coordinate | Tissue/cell |
SE_34128 | chr7:73252512-73254101 | HCC1954 | SE_34313 | chr7:73252271-73253728 | HCT-116 |
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| Number: 1 | ID | Chromosome | Start | End |
GH07I073838 | chr7 | 73252663 | 73253730 |
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Enhancer Sequence | TCTTGCTCTG TCACCCAGGC TGGAGTGCAA TGGCATGCTC TTGGCTCACT TCAGCCTCCG 60 CCTCCTGGGT TCAAGTGATT CTCCTGTCTC AGCCTCCCTT GCAGCTGGGA TTACAGGCAC 120 GTGCCACCAC GCCCGGCTAT TTTGTATTTT TTGTAGAGAT GGGGTTTTGC CATGTTGGCC 180 AGGCTGGTCT CGAACTTTTG ACCTCAGGTG ATCTGCCCGC TGGGGATTAT AAGCGTGAGC 240 CACTGTGCCT GCCCACCCCC CCTTTTTTTT CTTTCTTGAG ATAGGATCTC ACCCTATTTC 300 CTAGGCTGGA GTGCAGCAGA GCAATCATAG CTGACTGTAG CCTCCAACTC ACGAGCTCAA 360 GCAATCCTCC CACCTCAGCC TCCTGAGTAG CTGGGACCAC AGGTGCTCAC CACCACGCCT 420 GGCTAATTAA ACATTTTTTT TTTGTAGAGA TGGGGTCTTG CTATGTTGTC CAGGCTGCTC 480 TTGAACTCCT GGGCTCAAGG GATCCTCCTG CCTCGGTTTC CCAAAGTGCT GGGATTATGG 540 GGGTGAGCTA CTGTGCCTGG TGGGGAATTC TTGACGTAAT TCTCCTGGAT TGAGGAGACA 600 CCCTCCTCAC CACTCACCAC TCACCCACGC CTCTGCTGGA GGATGTGACT GTGTCTGAAT 660 GGACAGGAAG AAAGTTCCCA TGTGGGCTTT GGATCTTGGG CTATCCCTTC ACCTCTCTGG 720 GCCTCAGTTT CCCAGCTGGC ACAGAGAGGA TGATTATCTA ACATCACAGG AAGGCTGGTA 780 TGTGTGTTTG AAGTGCCCTA CAGTAAGTGC CGGCTGAATG GCCTTGTCAC CTCAGGTCCA 840 GGCACCTATA GTGTGCGTGC CCAGGGTGGC CCCAAGTGCA CTGAGAAGGA GAGATGGGGA 900 AGCCCAAGTG ACTGGTCTGG GAAGGTTTCC TGGAGGAGGG GGTAAGGAGA AGCAGGGTGT 960 TGCTGATAGA AGGGAGCGCA GTGAGAGGAG AGGCTCCGGA GCAGGGGAGA CTGTCACCCA 1020 TGGGCAGCCT GATGGGGCTG AAGGGCTTAG CAAGCACAGG TTGGGCTAGG AAGTCCGATC 1080 CTGGCTGCTT CACCCAGTAG AAAGTTCCTG TCTTCTTGGG CCCAACTTCG ACCTTTCCAG 1140 CTGACCCCAT CCGTGTCCCT GCATTTGTCA GCCTTCAGGG CTCCCCAGAT GCCTGCCCAG 1200 ACCTGCCCAG GCTTAGCCAC AGCCTCTGCT GGGCCTGGCA GAGACGGGAG GGAGAGGAAG 1260 CATTTTTACC TCTATGATTT CCTGTCCTGC AGCCAGCCAG CGCCTCCTCG TTCTCATGCT 1320 CAGCCCCTCT CCTTTCTGCC TTAGGGTGCA CCCCATGTGG ATTCCTCACC TGGTCTTGGA 1380 AATGCCTCTC TTCTCTACAT 1400
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