| Tag | Content |
|---|
EnhancerAtlas ID | HS133-00456 |
Organism | Homo sapiens |
Tissue/cell | melanoma |
Coordinate | chr1:17019080-17021230 |
Target genes | | Number: 16 | Name | Ensembl ID |
|
TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| HES2 | MA0616.2 | chr1:17019452-17019462 | GGCACGTGCC | + | 6.02 | | HES2 | MA0616.2 | chr1:17019452-17019462 | GGCACGTGCC | - | 6.02 | | TFAP2A | MA0003.3 | chr1:17020139-17020150 | CGCCTCAGGCA | + | 6.62 |
|
| | Number of super-enhancer constituents: 3 | ID | Coordinate | Tissue/cell |
| SE_34251 | chr1:17017869-17019700 | HCT-116 | | SE_34251 | chr1:17019986-17022004 | HCT-116 | | SE_68989 | chr1:17020022-17021951 | H9 |
|
| | Number: 3 | ID | Chromosome | Start | End |
| GH01I016692 | chr1 | 17019261 | 17019738 | | GH01I016693 | chr1 | 17020361 | 17020550 | | GH01I016694 | chr1 | 17020921 | 17021050 |
|
Enhancer Sequence | TTCTCTTCCT TTTTCTTCGC CTGTTCTTCG GGGGCCGGCC CAGCCTCCAG GCCGTTTCCG 60
AAGAACCTGT GCCTGAGGTC CTCGAAGCCG TCGCTCCAGC CGCGCCGGCC GGCCTCCACC 120
TCCTCCAGCA CCACGCGGTG GAAGAGGCGG ATGCGCTCCC ACGGGTGGCT GTCCAGCCGG 180
TGGAACATCT CGTAGCACAG TAGGTGGCGG AACTTGCGAT CCTCGCGGCT CAGGCCCATC 240
TCCGGTAGCT GGAAGTAGCC GAGCATGAAG AGGTCGAGCG TGAGGCTTTC GTAGCGCGGG 300
GGTGCGCCGC CGTCTAGGGG CGACAGGAAG TGCTGGGGCC AGTACACGCC GTGCGCCAGG 360
CCCGGGCTTG GCGGCACGTG CCGCCGCAGG CTCCGCCAGT GGTGCAGCAG CTTGCCCACT 420
GCCTGCCGCT GCCTCAGCAG CTGCCGCAGC CGTTCGTTGG GGCTGTGGGC CTCGCCCTTG 480
CTCACCGGCA GCCGGGGGGC GTCCGTGGCC TCCAGCTCCG GCCAGCACGG GCGGCCGTCA 540
CGCCAGGGAG CAGTCTGCCT AGGCGCGCCT GGTCCGCGGA AGGCCCGGTC CGAGGAAGGC 600
CCAGAGGCGC CAGTGCTCCA GGAAGAGGTA AACGATGCGC TCCTTGCGCA GGTCGAGGTA 660
GTCCTGGACG CCGCGCAGTT CCGTGCAGAG GGGCGGCCGG CGCGCCAGCT GCTCGGGCTC 720
AAGTAGCGCC GCCTGGCAAT CCTGTGCCTC AGGCGGGCCC AGGGTGTCCA GGGGCTCCCA 780
GTCGGCCAGC GGGCCGTGGG CGGCGGCGGC GCTGGGCTGG CCAGAGCCGG CCGCCACGTA 840
GTCCTCCTAC AGGATGGGCT CGCGGACCGG GGCGCCAGCG GACTGCGGGG GCTTGCGGCG 900
CGGACAGCGC GGGGGCGCCG CGTCCAGTGC GCGCAGCTCG TAGGTGGCGC GGTGATGCTG 960
CACGGAGACG CCGCACTCGA GGATCTCGCG CGCCACAGCC TCGCGGCACC AGTTGAGCCA 1020
GTGCGAGCGG CCCAGGCAAA GCGGCCCCGG CAGTCAGGGC GCCTCAGGCA GCGGCGCCAG 1080
CGGCTGGCCC GTGTCAGCGG TCGGCAGCTC CGCCAGGTGC GCAGGCCGGC CGCCCAGCGC 1140
GGCTAGCAGC GTGGCCATGC TCTTGAGCAG CGTGGAGATC TTGCTGCACC AGGCGGGCAG 1200
GCTGGCGGCG CGGCCATGCA TTCGGCGCGG GTCGACGGTG AAGCGCGGCT CCACAGGGCG 1260
ACGGAGATGG GCAGCAGCTG CTCAGCTCCA GTTGCTCCAG GCGCGCCTCC AGCTTCTGCG 1320
CCTTGTGCAG CACCTGCAGG TTCTCGATTG CTGCTCGATG CGGAGGATGT CGGCCTCGGT 1380
CATGAGCTCG CCAAAGGGCC AGAGGATGGC GTTGTGCTCG CGGGAGTACC TCCAGCCCTC 1440
GCGGGGGTAC CTCCAGCCCT CGCGGGGGTA GCAGCACGAG CTGGCGGCCG TCAGCTAAGG 1500
CGGGGAAGAC AAGAGAGGGG AGGGAGGCGC GTCTCCCTCT GGCCCAGCTC CCGCCGTGGC 1560
GCCAGGAACC TTTTGCATGT CCTGGGTGGT GTAATGGCTC CGCGGGGCTG CGTCTGCAGG 1620
GAGGGACCGC GTCTGGCCGG CGGGGGGTGA CGCTGGGGTG AGGCTTCGGC CTGAGCCGCC 1680
GCTCCAGGCT CTGGGCAGTG TCCACTTTGG TCGCTGGCGG GGGGCACGGC CGGTTGCTGC 1740
TCGCTGCTGC GGCGGCAAGA ACAGGCCAGC AGACGGGGTC TCCATGCCTG GCTTGTTCGC 1800
TCATTACACC ACCCAAGGAA CTTGCCAAAG GCCTTGAAGC TGAGAGGCGC GGTGGCCCGC 1860
CCCAACCCAT CCGAGGGCGG CTATTGTGAG GCCTCTCCTC CCAGACTCAT GACCCCTTCT 1920
CCAGCTCCCC TGTGGCCCAA GCCTTCCGCT CCCTGTGGTC AATGTTTTAT GTGCAGAATG 1980
AGAGGCCACT CCTCTCTTAA AGAGGCTGCA GCTGCAGCTT CCACTGAGCT GCCCACCCTT 2040
CCCCTCCCTT CGTCGTGCTG GACAGCTGGG CACCGTAATA TTCTCATTTG CTCACTTTTC 2100
TCCACCTCTG ATGTCCAGTT TTCCCCCCTG GGCCTGCCAT CGCCTCCACA 2150
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