| Tag | Content |
|---|
EnhancerAtlas ID | HS133-26173 |
Organism | Homo sapiens |
Tissue/cell | melanoma |
Coordinate | chr6:3810180-3812410 |
Target genes | |
TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| Foxd3 | MA0041.1 | chr6:3810780-3810792 | AAACAAACAAAC | - | 6.32 | | GLI2 | MA0734.2 | chr6:3810382-3810397 | TGCCCACCCACCATG | + | 6.05 | | Nr2f6(var.2) | MA0728.1 | chr6:3810565-3810580 | GAGGTCAGGAGTTCA | + | 6.22 | | ZNF263 | MA0528.1 | chr6:3811360-3811381 | TCTTCCCCTTTCACCTTCTCC | - | 6.03 |
|
| | Number of super-enhancer constituents: 2 | ID | Coordinate | Tissue/cell |
| SE_37041 | chr6:3807619-3810755 | HSMMtube | | SE_38003 | chr6:3803047-3810480 | HUVEC |
|
| | Number: 1 | ID | Chromosome | Start | End |
| GH06I003807 | chr6 | 3808101 | 3810527 |
|
Enhancer Sequence | GATGGACTCG ACCTGTGTGG TCATCACCTG GACTGTCCAG CCTGCTTCAG TGCATTGCTA 60
CATGCCCATT CCCAAAACTG ATACTGGAGC ACTCCACCAG GCCACCTAGT CAAGGTTACA 120
GCTTGACTCC CTGTGGCCAG GAGTCCCCAA CTACACATAG CCATGGGGCA GGGGAGAGAA 180
AAGCAGGCCT TCTCGGCGAC ACTGCCCACC CACCATGTTC CTCGGCCCGC CGCAGCCGCA 240
GCTATCCTTA ACCCCTCCTT GCAAGCTCTG TGTTTATAGT CTTGATCTCA GCCTAGGGGA 300
CTTCATTCAA AGCCCAGGCC CTTGGGCACG GTGGCTCACG TCTGTAATCC CAGCACTTTG 360
GGAGGCCAAG GCAGGCAGAT TACCTGAGGT CAGGAGTTCA AGATGAGCCT GGCCAACATG 420
GCAAAACCCC GTCTCTACTA AAATACAAAA AATAGCCAGG TGTGGTGGCA CATGCCTGTA 480
ATCCCAGCTA CCCGGGAGGC TGAGGCAGGA GAATTGCTTG AACCTGGGAG GCAGAGGCAG 540
CAACGGGCTG AGATTGCGCT ACTGCACTAC AGCCTGGGAG ACAGAGTGAG ACTCCGTCTC 600
AAACAAACAA ACAACAACAA CAACAAAAAC AGGCCCTGAG TTTAGTAGCT GAATCTTGCC 660
GTATTTCTTA CACCTAAGTT CTCAGCCCTA TTAACTGAGC TCCCAGGAAG TTTGCTCCCA 720
TCACGGTTCC CAGGATGGAC ACCTTGTTCC CCAATGGCTT GACCCATTCT CCCTCAGCCT 780
TCCCGGGATC TGCGTGGGGT CTCCTTTGCC ACTGCTGGGC TTTCCTGTGT CACTTGCTGC 840
CCCTGGCGCC TCTGCCTCCA TCCCAAGTCA TAGCTTTCTC TGTGGCCTGC CCTCCATGGT 900
GTGAACACTG CCCACTCACA GTCCCTGGGT GTTCTGCGTC CTGCTCCAGC TCAACTTTTC 960
CGCTGCCCTC TTTTGCCATG CTCTGGGGCA ACACCAGACT TGTCACCGGT TGCTATGGTC 1020
TGAACGTGTC CCTTTAAATT CCCGTGTTGG AAACTTAATC CCCAGTGCAG CAATGTGGGA 1080
AGCTACAGCC TTTTGGGAGG TGGTTGTGTC ACAAGGGCTC CACACTCATG GATGGATTAA 1140
TGTAGCTCTA AAAAGGGCTT GTGGGAGTGG GTTCACTCTC TCTTCCCCTT TCACCTTCTC 1200
CCATGTGAGG ACACACAAGA AGGCTCTCAC CAGATGTCAC CGCCTTGATT TGGGACTTCC 1260
TAGCCTCCAG GAGAATGAAG AAGTAATGTT CTGTTTTTCA TAAATTACCC AGTCTCAGGT 1320
ATTCTGTTTT AGAGCACAAA ACAGACACTG GCATTCTTCA TGCTACCGTG CCCTCCATGT 1380
GGCTCCTAGC CAAGGCTGTC CACAATGCAG CCTTGTGATG CCTTGGGATG CAGGGTCACC 1440
CTGCCATCAC TATGTGTGCC AGCCCTCCAG CTGGCTACTT TCTGGGTTCC TCCATGGGTC 1500
AGGCAGGAAC TTCAGCACAT CCTGCATATG ATGCAGGAGC TGCAGGACGC TTGGTGGGGT 1560
GCTCCACTCT GGCCCTCCCT TCTACCCCAC CATGCTGCCT CACCCTACTT ACTGCAACTG 1620
TGGGCAGTCA GCCAGTGTTT TAGCGCATTG GGCTGCTATA ACAAATTACC ATGGACTGGG 1680
TGGCTTATAA ACAACAAAAA GTGATTTCTC ACTGTGCTGG AGGCTGGGAA GCCCAAGGTC 1740
AAGGTGCTAG CAGATTCTCA GGGTTCTGGT GGTCGGAAAT CTGAGATCAG GGCTGCCAGC 1800
ATTGGGTTCT GGCGAGGGCC CTCTCTGTGG CTTGTAAGTG GCCATATCCT TGCTGTGCCC 1860
CCACATATTG GCGGACTGGG AAGCAGGGAG AGAGCGAGCA AACTCTCCAG TATCCATTGT 1920
TATAAGAGCA CTAAATCCCA TCATGGGAAC CCTGCCTGCA TGCCTCATCT AAACCTGACT 1980
GTCTCTCAAA GGCCCCGTCT CCAAACACCA TCGCACTGGG GGTTAGGGCT TCAATGTGTG 2040
AATTTTAGGG GGATACATGC AGTTCATAAC GAACGTCTAC CTTGCAGGGC TGTTGTGAGG 2100
ATTAAAGAGA TAGTGCCTTG GCCGGATGCA GTGGCTCACG CCTGTAATCC CAGCACTTCG 2160
GGAGGCTGCA GGCGGATCAC TTGAGGTCAG GAGTTTGAGA CAACCTGGCC AACATGGTGA 2220
AACCCTGTCT 2230
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