| Tag | Content |
|---|
EnhancerAtlas ID | HS133-22886 |
Organism | Homo sapiens |
Tissue/cell | melanoma |
Coordinate | chr3:126665100-126667430 |
Target genes | |
TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| SOX10 | MA0442.2 | chr3:126667037-126667048 | AAAACAAAGCA | + | 6.02 | | STAT3 | MA0144.2 | chr3:126666973-126666984 | CTTCTGGGAAA | + | 6.62 | | Stat4 | MA0518.1 | chr3:126666973-126666987 | CTTCTGGGAAACGG | + | 6.53 |
|
| | Number of super-enhancer constituents: 1 | ID | Coordinate | Tissue/cell |
| SE_61225 | chr3:126659718-126703478 | HBL1 |
|
| | Number: 1 | ID | Chromosome | Start | End |
| GH03I126947 | chr3 | 126666361 | 126666510 |
|
Enhancer Sequence | GAAAGCGCCC CACCTGGCTT CCTCTGACAT CTAGTGAATG AGGGTGCATC TCCTCTTAGG 60
GAAAGTGTGC ATTCTTTATT TTTTTCCAAC AAAGAAACAA AGAGGAATGG CCCTTTCTTC 120
TTTCCGTGTG TGTGAGAGAG AAGGGATAGT CCTGGACAAT CCTGTCACAC GCAGCCTCTG 180
CCTCACTAAG CAGCAGCCAG GGGCTCGTTT GTGTCTCAGG CCCTCTTGGG AGCAATGCAC 240
CCCCAGGCTC TCTCGCAAGC CTCAGCTCTC AAACAGGCCC CTCTCCCACC TGAGGGATGG 300
GGCAGCTGGA GCCCGGCATC CTGCAGTTGA TAGCAATCCC GTGTGGCGTG TTGATCGATG 360
GCAGGACCTC TGGGTTCCAC TTACCCAGGC TGAGTGGCAC ATCGTCAATA GCAGTCAGTT 420
AACCAAGTCC TTAGTAACCA GCTGGTCTCA TCAGCGCCTC AGCCCTAGCC ACGGGTTAAA 480
GCAGAAACCC CTCCTGAACA GCTAGATTGG ACCTGACCAA GATGAATGTC TAATTCACTC 540
GGAATCTCCT TACTGCTGCC TGTAATAAAA AGCCTGCTCC ATGTATTCAC CCCCCTGCTG 600
ATGTTTCTCT GAAATTAAGT ATCAGGAGGA CATATAATAG CCCAGTTCCA CACCAGGCCA 660
ATATTATCAG ATTGATGTCA GCAGTGATAA TAGGAGAAGG ATAAGTTGAT GAGATTCCAT 720
TTATTAAATA AAGTGAAGAG AGCACACAGA GGATTTGGGG CCACACGTGT GAGCAGGCGC 780
TGGGCGCGCT CCACAGGAGA AAGAGAGAAC AGGGCCTGGC GTCTGGTCCC GAATCCCTCT 840
TCTTGCCCAC CTGGGAGCTG GAGTGCCCGC CGTCATGGGA ACGACTTGGC CACCTACGAT 900
GTGTGCGCCC AAGATGGGAA GGTGCCACCC ATGCTTCTGC CAGGCTGGTC TCATGACAGG 960
ACGCTTCCGC TCACTTCTGT TTGCTTTTCT TCCCACCTCA TGTTGATGCT GCAGGCTGCC 1020
ATGAGTTCAT GTCTTCCTCT CTCACTTTCC TCCCTGTGGC TCCTGGGCTG GGAGCTTCCC 1080
GGCTGCCCAA TGGGAGTTGG CAAGCTTCTG CCCCATGCAG AGCCCTGCCT AATGTGGTTC 1140
GGGGCAACTG TCTTTTCTTT TTCTGAGTAC CCTTGGTTGT CTCTTTCAGA ATGTCTTGGA 1200
ATTTTCTAAT GGCAGAGTGG AGCTCATGTG GCGGTGCAGA GAGCAAGAGC TATGGAGCTG 1260
AGCACACTCC ACTCTTCCTA TCCCGGGCCC CTCTCACTGC TCTGTGACTG CGGGCCAGTC 1320
ACGTGAGCTG CCTGTGACTT ACCAACCCCG TCTGCAGAAC GGGGTGGGAA GGCCCAGCTC 1380
ACAGGGTTGT TGTGAACCTA GAACACAGGA AGCCCTGACA GGCAGAAGTT CCCAAGACCA 1440
CAGACATCCA GATCCACTCT CAAATGAGGC CGAATTTTCT GCCCGTGCTG TTGACCATCA 1500
GCTCCCCTCC CACAGGCTGA TCCTCATCCC AGATCTCTCC CAGTGCAGAA GACTTCCTGG 1560
GCAGCACCTG GCAGCAGCTT TAGGAACCGG CTCATAAGCT ACGGCTCCTC CCCTTTTCCA 1620
TTATGTGGGT TAAGGTGAGT CAGTTCATCT CTAAATAAAA TAACGCCTTA CAGGGGAGGA 1680
CAGAGATTGG AGACACCATG TGCAGACCCT GGCATGGAGC CTGGCATGTG GTGGGCATTG 1740
AAGTGTAGCG GCTATTGCTG ATGTGCGCCT GGGCCCAGCC ACCATGCCGT GGAAAGTGCA 1800
CACTGCTCTC AGAAAACGAT CAGAGATACA TTGGTCCCCC GGTCATTCCT GCCCATCCCC 1860
GCTCCCCACT CTACTTCTGG GAAACGGGTC CAACCCCTTT GCAGCATGCC TGATGACATG 1920
GGTTTCCCAG GGCTGCCAAA ACAAAGCACC ACATGTCAGG CCTTTCAGCC CAGAAACTTA 1980
TCCTCTCACA GTTCTGGAGG GCAGAGGTCC ACAATTAAGG TGTTGGTGGT CCAGTCTCGC 2040
CCTCAGGCTG GAGGGGAAAT CTGTTGCAGC CCCTCCTAGG CTGCTGGTGG TGCTGGCATC 2100
CTTGGCATTC CGGGACACAC ATACTGTTGG GCACACACAT CGCTCTACTG TCAGCCTCGG 2160
TCCCCATAGT GCCTCCTCCC TGTGTTGTGG TCTCTGTGTC TCCTCTCTTC TTCACAAGAG 2220
AATATGAATG GGATTCGTAC TGGATTAGGG GCCCACCCTA CCCCATATGC CCTTGTCTTA 2280
ACTAATCACA TCTGTAACAA CCCTGTTTCC CAATAAGGCC ATGTTCCGAG 2330
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