| Tag | Content |
|---|
EnhancerAtlas ID | HS133-08841 |
Organism | Homo sapiens |
Tissue/cell | melanoma |
Coordinate | chr13:109807410-109810140 |
SNPs | | Number: 1 | ID | Chromosome | Position | Genome Version |
|
TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| ZNF263 | MA0528.1 | chr13:109809780-109809801 | TCCCTTCCTTTTCCCTCCCCC | - | 6.47 |
|
| | Number of super-enhancer constituents: 2 | ID | Coordinate | Tissue/cell |
| SE_36306 | chr13:109806480-109811018 | HMEC | | SE_64525 | chr13:109806086-109811668 | NHEK |
|
| | Number: 1 | ID | Chromosome | Start | End |
| GH13I109153 | chr13 | 109805787 | 109815118 |
|
Enhancer Sequence | TTTCTGTGCA TTTTTGGGTA CTGAAAACCT TATTTATACT GACAGTCATT TTTTAGCTTT 60
ACTATCAATG CATTCTTCCC TTGCTCAGCA CATATGTTGT TGAAGACATC GCTCTGTTTC 120
CTACTTCAGT TGGTGTTTTC TAGCACAAAC CATCTCCTTC GACTTGGCGG GGGGGTGGGT 180
GACAAGAGTT AGGAGTGAAG GAGGAGCAGA CATTTCCATT CCTCCCCGCT TAACCTGGAG 240
GATAAGTATC TGCGGCACTC GCTACCAGAG AAGAATGCTT AAAACATAAG TTCAAGAGGA 300
ATTTCGATCT ACTCCAGGGT GGTGATTTCA TAAGGGGTTA TTAACAAGTA GGAAGGAATG 360
TCGGGAGCCC AGCCCGAGAC ATTTAAAGTC AGTAGAGGGC CGGGCAAATC CAGTTTCTCA 420
GCACACGCAA CCTTTCCAAG GTCTGCAGTG ATGTATTTTT CTGTTTCTTA AGTAATCAAT 480
GCTTATAGAA ATATGACCTG TCCACATAGT GTGGGTAACA GCTGTGTCAC AAGAGTAACT 540
GCCTGGGAAC CCAGTTCTCT TCCCAGATCT CCATCACCAC TAGACTCAGA CGCCCTCTCT 600
TGATATATTT CTGCAAGCAT TCACAAAGGG ATGATAAAAT CTGTTGCACG TTTTCAAAAG 660
GCAATTAGAA TTGTGCTGTT CAAAACATGC ATAATTGCAG TGTGTCACCT CCATGAGTTT 720
AACACATTTC CCCTGTAGCA GTCTCCACTC TCCTCACATC CACCCATCTC CACTGAACTC 780
TCTCTTCTTG AGTTTCAGAT TAGCCTCTGT GGTTCTTTAC ATCTGAAATT CGTCTTTCTG 840
AGAGGCAATA ACACAAATAT TTGGATTATG CTATCATGGA AAGGAAAGAA AATTCTATCA 900
TGTAAAAGAA AAAACATATT ATGTAAAAGA AAACAAATCA CTTCCTAGAA GCTTATAAAG 960
TAGGATGCAG GTCGACTTGA GAGGGGTGTC AAAGCCCTGT TTGCATTTCT TCCTCATGTG 1020
CAGTAATACA GGGTTTCAGA GAAATCTATA TTTTAGAGAT TTAAAAGGAG TTGCCCTGTG 1080
TAACACAAAC TAGATTTGGT TTAACACAAG CTAGACGCCA ATTTCAGGTC GAAGTGCTTG 1140
TATCCAAATT TAATTACGCA CCATCTATGT GTATCTGCAA GCGCTGTCGA GCTGCGACTT 1200
CTAAATTTTA CAAACGAGAA CTTGAGAAGT GGTGGGAGCC TGCCAGGCAC CTCTCTCTGC 1260
ATTTGTACTT TTCCTTAATG CCAAGTAGGA AAAAACAAGC ACATTCCCTT CATGCAATAG 1320
CCTTTCTGAA GAGGAATTTT CCTATAGAGT TTCAGAATGA GTTATAGCCA GTATGAGTAA 1380
TGAGTTTAAA ATGTATTTTC ACATTTTTTA TGCCTTACAT AGCACTCTCA GTATTAAGTC 1440
AGCCAAACAG CTATAGTTTG TTTTTCTCCT GCGTTACTGA AACCCGGATC CCATCTCATA 1500
GGATTCTAAA ATACACTCTA ATCTGATCTC TAGCGCAGGT ACCTAAGAGA AAAGTGGTGT 1560
TTTCAGCATC TTGTTGGGGA AACATTCCAT GGCTCCTTTC TCTCCCCTGC TTCCTGGCCT 1620
TTCCCCAGCA CTGACGCTGT CAGCCGCCCT GCGTGCCACA CAGTCCTGCC CTCTGCCAAG 1680
GCTCCTGGCC TGCAGCCCCT CCTGCAAGCC CACATCTGCC CTCCTGCACG CCCACATCTG 1740
CCCTCCTGCA CGGCAGTCAC CTGGGCGTCC CCTCCTGCTA CCTCCTCACA CTCGAGAGTG 1800
TCTCTTCCTT GAAAATTTCT CCTTCCTGAG AGATTTTTAA GTCTCTCCTA GCTGTTTCCT 1860
TTCCAGTCCT AATAAATTCT CTTCTTCAAA AAATTGCCAC TCAATTTAAT CCTCAGGCCT 1920
GCGGCTGTCA CTTCAAAGTC AACAAGTACA ACCCCAGATG CACCCTGCTC TTCAGGTGGG 1980
AGCTGCTGCT CTGAACCACG CCCCAGCTGT GGTCCCCATC AGGTCCCAGT TCTCCCGCTC 2040
AGTGGGATTG AACTCAGCTT CCTCCTGCCT TTCCACTCCT CCTTCTGCTT CCCCAGCCTC 2100
TCCCCTGACT CTCTTTCTAC TTCTAATCTC TCCTCAAGGT CCATTCAGCT GTATACTTTC 2160
TTTGCTAGAT TAGTATTTAC AAAAAAAAAA AAAAAAAAAA AAAAAAACCT TATTCTTCAC 2220
AGCATGCCCT TGCTCAAAAT ACTTGCTGGA ACCCAGTCCT GTGATGCTCA TAGACTCCAA 2280
AGCTCTCTGC TCCCACTTCC CGGTGCGGAG GTGTGGGCAG AGCCAGCCTC CCCTCCCTCA 2340
CGAGTGCAGT CAGCTCTGCC TCTGCGGCAT TCCCTTCCTT TTCCCTCCCC CTCTCCACAT 2400
TCCGTCCTCA ACTCAAAATC CACTGCTTCT TCCTCCTGCC TACACAACAA AGGCTCACCT 2460
GGCTGCTCCA GCCCACTCTG ACCTCTCCTA AGAATTCCTA GAGCATTTTG CAGAGCTCCC 2520
ATCCCAGCCC CCTGGCCCTT TGCAACCTTA ACACATGCCT TGAAGGCACC TTGAAGACAG 2580
TCCCCCTTAG AGCTGAGTCA CCACAGAGAA GCCTGGGGAA AAGCACCCCT TAGAATGCAC 2640
CCTGGATGTC CCTGTCACAT GGGTTGGCAT TATAAGTGTC AAAGGCTTTA ACAAGTGAAT 2700
AAAACCGTCA AAATTAGCTC AGCTGAGCAG 2730
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