| Tag | Content |
|---|
EnhancerAtlas ID | HS133-16474 |
Organism | Homo sapiens |
Tissue/cell | melanoma |
Coordinate | chr2:20672810-20675350 |
Target genes | |
SNPs | | Number: 1 | ID | Chromosome | Position | Genome Version |
|
TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| Foxd3 | MA0041.1 | chr2:20673443-20673455 | GTTTGTTTGTTT | + | 6.32 |
|
| | Number of super-enhancer constituents: 3 | ID | Coordinate | Tissue/cell |
| SE_04358 | chr2:20674697-20675781 | Brain_Anterior_Caudate | | SE_31673 | chr2:20672316-20673499 | Gastric | | SE_41814 | chr2:20672668-20673385 | LNCaP |
|
| | Number: 1 | ID | Chromosome | Start | End |
| GH02I020471 | chr2 | 20671537 | 20675718 |
|
Enhancer Sequence | GACTCAGAAC CAAGGCCTCT TGAGTGGGAG AGATCTCAAA GTTGACTGAG CCCAGCTTCC 60
CATGAAGGGT ACTTCCCAGA GCAGTTCTGC CAAGGTGCCA CCCTGGCCCA AGTTCCACCC 120
CTCCAGAAAC AGGGCCTGTG TGCCCTCAGG AGAGCACCAT CTCCAGCCTT GGATAAGGCT 180
GCCTTCCTGT AGGGAGAGGC CGCCCCCCTG TTCCGTCTAC TGAGGGGCCC CAGCTCTGCC 240
ATCTGGAGCC TCACCCTGCT CTCCTCTGAC TGTGGACGTT TAAGTCTAAT ATCTGCTGGG 300
CTCCAGGCCA GCCACCCTTG GGTCAGCACT TGGCTGTCCC TGCTAGAAGT GACTGTGAAG 360
GCTTCACCCT CCTCTGTCCA AGGCGGCTCC TGAAGGAGCA AGTTCCAGAG CTGGAACACC 420
AGGACCCCCA AACTCCAGCT GTAGACTGAC CAATGCCAAG CCAAGTAGGG CTGCCATCTC 480
CCTGGCCTTT TGGGATTTCC TATCTTCTGC CTTGGAAACT CCACCATAGG CACGTCTTCT 540
TAGCCCAGGC TTGAGGAGCC ACCCCAGCTC TATTCCTCTT CGAGTCCTCC CATCTCAACA 600
TGAATTCTAG CTGGGAGCAA ACATTTTCTA GGTGTTTGTT TGTTTTGAGA CGAAGTCTCG 660
CTCTGCTGCC CAGGCTGGAG TGCAGTGGCA CGATCTTGGC TCATTGCAAC CTCTGCCTCC 720
TGGGTTTAAG TGATTCTCCT GCCTCAGCCT CCCGAGTAAC TGGGATTACA TGCGCCACCA 780
TGCCTGGCTA ATTTTTTGTA TTTTTAGTAG AGACGGGATT TCACCATCTT GGCCAGGGTG 840
GTCTCAAACT CCTGACTTCA AGTGATCCAC CCACCTTGGC CTCCCAAAGT GCTGGGATTA 900
CAGGTGTGAG CCACCATGCT GGGCCCTCTA GGTGTTTTGA AAATAGCTGC AGGACACAAA 960
CCACCAGGCT GCTTGCTGCC CTGGATTTGG GGGGCTTGAG CTTGGGGATC CAGGGTCACG 1020
GGCCCTGCAG GCTCAGCCCA CCCTCTCAGG GCTGTGGGTC TCAGAAGCCT GTGTTCAGGT 1080
AAGCAGTAGC AGGAAGTGGA GATCTGGAAG CTGGAGCAGG AGCCCCAGCT CCACTGTCTT 1140
GTGGGGTTTG ACCATTAACT GCTAATCCTC AGGCCTGTGT CTGGGCAATA GACTGAGGCC 1200
AGAGCAAGGC CGGTCACAGC ACAGCTGGGG GAGCACTCAG GGCAGAGTGT GACCCTGAAG 1260
TCCCAGAGGT GACCTTGGGA GGACTGGGCA GTGTTTGCCT GGACTGTTCC TTAATGAGCT 1320
CACCCAAGCA CATGGTCTTT CCCTTCCACA CACTCACCCA CATTTATATT CTGCAGAGTG 1380
ATCCTGGCGA AAATGATTCT TTCATTGCCT GCCTAACCGG ACGAGCAAAG CCCACAGGGG 1440
TTATTTGGAC AAGAGTATAA AAGATCTCAA GAATGTGACC TGACCCAAAG AGCCCAAAGG 1500
GAATAATGGA AGCTTCTGCC AGGCCTTTGG GGATTAAGTG ATGGGTATGG GGGCGGGTGG 1560
ATGACTCTGT AATGGTCCTA TTTCTGATGC ACCAATAGGG ACACAGTCTT AAAACAGGAA 1620
GAAGAACAAA GGGGAATGAA CGTGCTCTGC AGTGGGCTGG GGAGCAGGGC AGGCTGATCA 1680
CGCTTCAAAA AGCACTGTTT CCTCTTCCTT CACTATACAT CATGACTCTG GGAATTAAAG 1740
TTTGTGCTTT GAGCGACGTG TGTGTGTGCT TATGTGTGTA TAAATTGTGT GCCTCCATGT 1800
GTGGATTTGT GTCCCTTTAT ATGTGTGTGT GTTTGAGCGG ATCATTATCT GTTTGATGAC 1860
CTGAGAGAAT GAGGACTGTG GGTCTCAGAA GCCCATGTTC AGGTAGGCAG TTGCAGGAAG 1920
CAGAGATCTG CAAGCTGGGG CAGGAGTCCC AGCTCCACTG TCTTGTCAGA TTTGACCATT 1980
AACCACCAGT TCTCAGGGTT GTATCTGGGC AAGAGGCTGA GGCTGGGGCA AGGCCGGTCA 2040
CAGTGCAGCT GGGGGAGTAC TCAGGGCAGA GTGTGACCCT GAAGTCCCAG AGGTGACCTC 2100
ATGAGGACTG TATACTGGTA GGAGACCTAG AAAAAGAACG AAATGTCCTG TCCCTAAGCC 2160
CAAGCCCAAC TTGACTAGTG TCCCTAAGCC GAAGTCCAAT TTGACTTATT CTGCTGATCA 2220
CCCCTGCCTT CCCCCAAGGC CAACAATGGC ATTGGACTAG AGCAAACAAA ATGATTCAGA 2280
CTTTGGGAAA TAGACTGTTC TGGATTCTGG TGTCTTCCAG ATTGCCTGAC TGGGGAAGAA 2340
AATGGAAAGG GTGGAGCACA CTAGGGTTAG ACCATTTGCT CAGGGAGGTG GCTTGGAGTT 2400
TCACACTGAA GAGATGAGAA TGTGGAGCTG CTCTAAGGGA ATGTCATACA ATGAGGACGA 2460
GCTCTGTTCA GCCCTGGGGC TGCATGAAGA AGAAAAGCTG ACCAGAAATC AGCCTCTCCC 2520
TCAGATGGGG TGAGGATGCT 2540
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