| Tag | Content |
|---|
EnhancerAtlas ID | HS133-26461 |
Organism | Homo sapiens |
Tissue/cell | melanoma |
Coordinate | chr6:18042560-18044410 |
Target genes | |
TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| IRF1 | MA0050.2 | chr6:18043725-18043746 | TCTTTCTTTCTTTTTTTTTTT | + | 6.25 | | Klf1 | MA0493.1 | chr6:18043031-18043042 | AGGGTGTGGCT | - | 6.02 |
|
| | Number of super-enhancer constituents: 1 | ID | Coordinate | Tissue/cell |
| SE_64611 | chr6:18042943-18043865 | NHEK |
|
| | Number: 1 | ID | Chromosome | Start | End |
| GH06I018042 | chr6 | 18042656 | 18044230 |
|
Enhancer Sequence | ACATGGCTTT TTGAATGACA CTCCACCTCT GCCTCTCCAG TCCTGCAACA AAGAGAGCAC 60
TTCTCTTCCT TTGTCATTTT CCCTGTGGTC TCTTAGGACA CGCTAGGTCC CCTGCTTCTC 120
TTCTTATATC CTCTCCTCTC CCCAAGGGGA GTTTCTTCTG CATATTCATA GTTTCTGCTC 180
CTTCTTTTCC TTGGCTTGGC CATCCTGGAC ACAAACCTAG TTGTGATGGC AGCACACTCC 240
ATGGAGCTGG TGAGAGCCCC ACCCCTTCTG AGTTGGGACA GGAGCTCCCC GGGTGCTGCT 300
ATAGCCGCCC AATGCAGCTG CAGACCCAGG CCTCCTGCTC TACAGAGCAG GCAGGAACCC 360
CACTCTCCTG GGTGGGGCTA CAGGAACCCA AACTGTAGCT GTGGATTCAT CTGAGCCTCC 420
CTGTGCTCTT GGGGGAGGGC TGGCAGCAGG CAGGATCTGC CTTTCTGGGT GAGGGTGTGG 480
CTGCAGCCAC CCTCCTAGAT GCGGGAGCCA GGTGTCTCTG CAGCCTGCAC CCTCAGCAGC 540
CCCAGGAAGG ACCCCCTCCG CTGCCCTGAG CCACCCACTC CTCTGAGCTG TTCTAACACT 600
AAATAAAACT CTTCTTCTCC ACCCTGCGCT TGTCTGTGTA CCTCATTCTT CCTAGATGCA 660
GGGTGAGAAC TCGGGCAAAG GTGCTTCGGC CGCAGAGGTT TCCCACCAGA AAAATTGACA 720
CCCCAGAGAT CCTGTAACAC TTGGACATCA GTGTCTGCAT CCTTTTGTTT TCTGTTCTTT 780
CTCCTGCTAA GTGACCCCTT TTCTTGTTAC TTTTCCATTC AAGCTGCTGG CAGAAAGAAG 840
CTGTCTGGCC ATGTTCAGGC TAGAAGTCAC AGTCAGCTCA TACCTGCCTA GGTCAGAGGC 900
TCCATCCGGT CCCACATCCA TAAGAGGCTG GTGGAAAACA TGCTGCCTAA CCCCACCACT 960
TTGACAAGTG GATGTCAGTG GGCAGGGCCC ATGGAGCCTG CTCAGCAGAG CACTGTTGTT 1020
CCTGGAGGCC ATGCTGACTG CAGCAGTCAA GGCTTTAGCT GCTTTACCAG TGCTCCCCTC 1080
CAGAGCTCCG TGGCAGGGTG AGTCATGCTG TGGGAATCTC ACACTGGAAA TGGCCAAAAA 1140
GCTTCTATTT GCTTCAGTGT TAGTTTCTTT CTTTCTTTTT TTTTTTTTTT GAGATGGAAT 1200
CTTACTATGT CACCCAGGCT GGAGTGTAAT GACTCGATCT TGGCTCACTG CAACCTCCGT 1260
CTCCTGGGTT CAAGCAATTC TCCTGTCTCA GCCTCCTGAG TAGCTGGGAC TACAGGAGCC 1320
TGCCACCACA CCCAGCTAAT TTTTTGTATT TTTAGTAGAG ACGGGGTTTC GCCTTGTTGG 1380
TCAGGCTGGT CTCGAACTCC TGACCTCAGA TGATCCACCT GACTCGGCCT CTCAAAGTTC 1440
TGGGATTATA AGCATGAGCC ACCACGCCTG GCAATGTTAG TTGGTTAGCC TGAGGAAACT 1500
GACACTTTTC TGAGGGGTAG CTAGCATGGC AAGAAATTAA ATGAGCATTC TTCTTCTTCT 1560
TTTTTTTTTT TTTTTTTGAG ACGGAGTCTT GCTCTGTTGC CCAGGCTGGA GTGCAATGGC 1620
GTGGTCTAGG CTCACTGCAA CCTCTGCCTC CCAGGTTCAA GCTATTCTTC TGCCTCAGCC 1680
TCCCGAGTAG CTGGGACTAC AGGTGTCTGT CACCGCGCCT GGCTAATTTT TTTTATTTTT 1740
AGTAGAGAGG GGGTTTTCAC CATGTTCGCC AGGCTGGTCT CGAACTCCTG ACCTCAAGTG 1800
ATCTGCCTGC CTCGGCCTCC CCAAGTGTTG GGACTACAGG TGGGAGCCAC 1850
|
