| Tag | Content |
|---|
EnhancerAtlas ID | HS133-26233 |
Organism | Homo sapiens |
Tissue/cell | melanoma |
Coordinate | chr6:7691580-7692960 |
Target genes | |
SNPs | | Number: 1 | ID | Chromosome | Position | Genome Version |
|
TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| FOSL1 | MA0477.1 | chr6:7692615-7692626 | GGTGACTCATG | + | 6.62 | | FOSL2 | MA0478.1 | chr6:7692614-7692625 | GGGTGACTCAT | + | 6.14 | | JUN(var.2) | MA0489.1 | chr6:7692611-7692625 | GGAGGGTGACTCAT | + | 6 | | JUNB | MA0490.1 | chr6:7692614-7692625 | GGGTGACTCAT | + | 6.32 | | JUND | MA0491.1 | chr6:7692615-7692626 | GGTGACTCATG | + | 6.02 |
|
| | Number: 1 | ID | Chromosome | Start | End |
| GH06I007690 | chr6 | 7690848 | 7693281 |
|
Enhancer Sequence | CCTCCTTCCT CTGTCCACTG ACTAGCTGTC TCAGAATTCT TTTTTTCCTT CTTTGAATTT 60
TTTTTTTTTT TTGAGACGGA GTTTCGCGCT TTTTGCCTAG GCTGGAGTGC AATGGCACGA 120
TCTCGGCTCA CCGCAACCTC TGTCTCCCAG GTTCAAGTGA TCCTCCTGCC TCAGCCTCTG 180
AGTAGCTGGA ACTACAGGCA CCCAGCACTA CCCCTGGCTA AGATTTTGTA TGTTTAGTAG 240
AGACGGGGTT TCACCATATT GGTCAGGCTG GTCTCGAACT CCTGACCTCA GGTGATCCGC 300
CTGCCTCGGC CTCACAAAGT GCTGGGATTA CAGGCATGAG CCACCACGCC CGGCCGCTGT 360
CTCAGATTTC TGATTCCTCA TTCCTATTTG GCCAGCCTGG GTCAGGTGTC CACCTTGGGA 420
TGAGCAGAAT GCACTAACAC AGATAAGGCT GCCTGCCAGG CCCCTCCGTG TGGTGAGATG 480
ACGGCCTGGT AAGCACGTAG TTCTTAGAGC ATTGAGGCTA AGATGGCCCC CACTGAAGGC 540
ACCGTGAAAA GGGGATTTTC AGCCCTGGGT CATGATCCTG CTCCAAGGTG CTCCGTCGTT 600
CTGGGTTGCA GCCTATTGGG GAAATGCCTC CATGGGCGAG ACATCTGTTG CCAGTGCCAC 660
CCCCAGCTCC TCCCATGGTC CTCAGGTGTG GAGTGTGAAG GGAAAGATGT CAGGAGGGGG 720
AGAAGCAGAT GACATGGGTA AGAGGAGAAT TCTTACTTCT ACGTGGCTCC AACGGAAATT 780
TGCAGCCATA AAACCCAAAG GAGGTATTTG CTGAATCACA GGCACATTTT TCTGGCGTTG 840
AAAGCTGAAC TGGGCAAGGA CGTTAATGAG AACTAGTCCA CAATGATCTC TTTCAAACCC 900
GAATCTCTGT GCTGGTGATC TCCACAGGAG CCAGGGAGCC GCCTCCCCGA GACGAGATAG 960
CACATTCCCA AGCTTCTCAG ACTCAGGTGC CCGCTCTCTG TTGACTCTCT GCATCCCCAC 1020
CCTTTCCTCC GGGAGGGTGA CTCATGGTGC TGGGGCGGCA GTGTCTGAGG TCTGAGAGCA 1080
AAGTCAGAGA TGACTCTTTT GGGGGCTTGA AACTGTCTAT TGCAGCGAGG AGTCCTTTCG 1140
GTCTCACCCT TGAGGGTGCA TCTATCAGAG CTTTTGTCTG TTTTACAACT TCCTCCTAAA 1200
CCTAGAACAA TGGATTTAGA AAAGGGCAGG AAATCTATGC CTGTCTACTC CAGGGAAGGG 1260
GGCGTGAGTA GCATGGTTGG TGCCTTTTAG GTTAGGTCAT TTAATACAGG CTGGGGCTAG 1320
TGGGTTTGAA AACTGGAAAA TTTCAGGAGG GTCTCACCCC AAGTGCCCTC AAACTTCCCA 1380
|
