| Tag | Content |
|---|
EnhancerAtlas ID | HS133-13686 |
Organism | Homo sapiens |
Tissue/cell | melanoma |
Coordinate | chr17:78921840-78923240 |
Target genes | | Number: 30 | Name | Ensembl ID |
|
TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| KLF14 | MA0740.1 | chr17:78922076-78922090 | TGAGGGGCGTGGCC | - | 6.17 | | SP1 | MA0079.4 | chr17:78922077-78922092 | GAGGGGCGTGGCCAT | - | 6.32 | | SP3 | MA0746.2 | chr17:78922077-78922090 | GAGGGGCGTGGCC | - | 6.18 | | SP4 | MA0685.1 | chr17:78922075-78922092 | GTGAGGGGCGTGGCCAT | - | 6.04 |
|
| | Number of super-enhancer constituents: 1 | ID | Coordinate | Tissue/cell |
| SE_53829 | chr17:78922685-78923339 | Spleen |
|
| | Number: 1 | ID | Chromosome | Start | End |
| GH17I080948 | chr17 | 78922686 | 78923339 |
|
Enhancer Sequence | TGTTGCTGAT GAGAAGTCGC TGTCAGTCCC ACTGCACTTC CTGTGGAGAC TAGAGAGCGC 60
TGGGCGGGAG GCAGGCGGGG GAGGCCAGCA CGGCTGAGAG AAGTGAAGGC CGACACCCGG 120
ATCCCACCCA GCCTGTCCCT GTCGGCCGCA GCCCCTGGAC ACCTGAGCCT CTGAGAGTGT 180
CGAGTCGGTT GTGCTGACAA GTGCGCAGCC CTCTCAACGC GGTTGCGGGC TCCTGGTGAG 240
GGGCGTGGCC ATGGGGACGT GTCCTCGTGC AGCCCCTCCT CCGAGCGCTG CCCCCTCAGG 300
ACCAAGTAGC ATCAACCGAT GTCGAAAGCC CGTCTTTGTC CCTGTAGCTG TCAGACGTGA 360
CCGGGAGGAG ATGCATAGTC GGGGCAGGGG CCGGTGGGGG CAAGGGACCA GCCAGGCTCA 420
GCCAGCGGTT TCGGAGAGAC CAGATGTGAG CATCTCCCAA CACCAGAGGG AGAGGGCAGT 480
TCCTTGGCTG AGAGAGCGAG CACTGGAGCA GGGCCAGGGT CCTTTGCAGA ACGGGCTCCA 540
GACAGCAGTA GAAGGGCTCC AGCTCCAAAA CCAGGAACGT TTGGTGTATG CGATGGAAAG 600
CAGAGAGCGG GACAGGCAGG TGGGTGGAGG TGAGGCCGTC GTCCACCAGG GCAATCAGCT 660
GGGGCTTGAA GAGCGCCTGA GGGTCACGCA GGAGGGGCTG GTGAGGCCAG GGGGTGCGGA 720
TGTGGTTCCC GGAAGGCTCA GAGTGCCCGC ATGCTTTCCC CACACCCAGG CCGACCTCCC 780
TGCCTGTCTG CTGGAGGATG CAGAGGGCCG TTTCCTCCAT TCTAAGCCCT GAAGAGCAGG 840
GCAGTGCGTC CCTGCCCACG TCTTAGGCGG AGAGCCCAGA CGTCTGCATT GTCCCTTCAA 900
GTCAAGGCTA CTCTCTCTGT GGAGCACAGA GAGGAATGGG GCGGAGGGTG CTGGTGTCCT 960
CTGTGAAGCT GGCCTTTCGT TCTGCTCCCT GGCACAGGCT GGCTCACCAG AGGGTAAAAC 1020
GCAGCCCCAC CCACCCAACC GAGCTTCACC CGCCTGCCTC CCTCCAGGGA ACCCGATGCC 1080
CTGGAGCTGG AGGGAGGAAG GGCAGCCCCG GCTCCCAGGG CAGCCAAACC TCAGAGTTGA 1140
GCTCTGTGGC CAGGGTGGGA CAGGATTGTG GTCTCCCATC CCCTGGGCTG CGACTCCTCC 1200
TGCTGGCTCG CCCAGATATG GATCTGAGGA CAGAGTCCAG TCGGTGGGCA CCCAGAGATC 1260
TGGAACCACG GGTAGTGAGT CAGGCTGGCC GCCCAGGGTC ACTGCAGCAC GTCTGCCAGG 1320
AAGGGCTCTT ACCACCACGC ACAGAGCACA GGCCAGGCCA TCGAGGGGCC TGGTTCACAT 1380
CCTTTCCTCT CTCCCTCCCC 1400
|
