| Tag | Content |
|---|
EnhancerAtlas ID | HS133-32110 |
Organism | Homo sapiens |
Tissue/cell | melanoma |
Coordinate | chr9:115603010-115604660 |
Target genes | |
SNPs | | Number: 1 | ID | Chromosome | Position | Genome Version |
|
TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| SPI1 | MA0080.4 | chr9:115603791-115603805 | GAAAAGAGGAAGTG | + | 6.92 | | TCF7L2 | MA0523.1 | chr9:115603639-115603653 | AGACATCAAAGAAA | + | 6.44 | | Zfx | MA0146.2 | chr9:115603285-115603299 | CCCGCCTCGGCCTC | + | 6.01 |
|
| | Number: 1 | ID | Chromosome | Start | End |
| GH09I112841 | chr9 | 115603641 | 115603790 |
|
Enhancer Sequence | GGCCTCCCAA AGTGCTGGGA TTACAGGTGT GAGCCACTGC GCCTGGCTGA TATTTCTTTT 60
TTTTTTTGAG ACGGAGTCCT GCTCTGTCAC CCAGGCTGGA GTGCAGTGGC ACGATCTCAG 120
CTCACCGCAA GCTCTGCCTC CCGGGTCCAT GCCATTCTCC TGCCTCAGCC TCCTGAGCAG 180
CTGGGACCAC AGGTGCCCCC CACCACGCCT GGCTAATTTT TTGTATTTTT TTAGTGTCAG 240
CCAGGATGGT CTCGATCTCC TGACCTCGTG ATCCGCCCGC CTCGGCCTCC CAAAGTGCTG 300
GGATTACAGG CGTGAGCCAC TGCACCTAGC CCTGGTATCT GTTCTTAAAA ATAAGTTTTT 360
ACAATTCCTG GAGTGTCCGT GGATTTGTCT CTTATGTATA CACACCCTTC ATCAAATATT 420
CTCTTAACCT TGCCAGATGA AAAATCCAAT GCATACACAG CACTGGGATA CTATAGTACA 480
AATTACTCTG TTTTTTTTCC TGTGGCAAGT ATGTTAGTAC TTAGTATATA TTTGTATTTG 540
AAGCACGATT TAAAAATGTC ATATAGCAAG GATTTATCTG GCATCTATAA AACATTACAC 600
TGGGAGACAT AGCTTGTGTA ATTTAAGTTA GACATCAAAG AAACATTTGT TTGCTCTTTC 660
TTTACCCCCC ATGTGTGGGG CATATGTATG GAGTTTCTTG TTTACTGAGC CTGAAAAATC 720
AGGTCAATCA GGCTGAGTGA ATGGGATTGA TTGTACACAG TCTTGTCTGG GGAAGGGCAT 780
GGAAAAGAGG AAGTGTGGAC TGGCAGTCTC TGAAACCCAA GCTCTATCCC CGATAGTAGC 840
TGAGCTGAGT CCAATTAATA AGAAACAGGG CCACTGCTCC TCCACTTTTC ACCAGGAAAA 900
TGTCTCTGCA GAGTGCCCTG GGCACGATAG GAGTGATTGG ATGGCAAAGC AAAGACTGTG 960
TCTGGGATTA TCAGGGTCTG TGTGGCTGGG ACTAAAGACA CCAGGAGAAT GATAGATGTC 1020
TTAAGTGGCT TGCCCACCTT TTCACATTGC TGCTCTGTAA GAATTTTTAA GTATATTTTC 1080
TTCCTCCGAG AGAGTCATAT AGTTCCATTT CCAAAATGGC TTTCTGATTT TTGAAACTTA 1140
AGTAGGGCAG ACTTTGCTGT GCAGTATGGA AACTAAGCGT GGAGCAGAGG ACTTGCCACA 1200
GGCCTGGCTG TGGCCTGTTC TTTATTTTTT GGAGATGGAC TCTTGCTCTG TCGCCCAGGC 1260
TGGAGTGCAG TGGCACGATC TTGGCTCACT GCAACCTCCA CCTCCCGGGT TCAAGTGATT 1320
CTCCTGCCTC AGGCTCCCGA GTAGCTGGGA TTAGAGGTGC ACATCACCAC GCCTGGCTAA 1380
TTTTTGTGTT TTTAATAGAC ACAGGTTTCA CGACGTTGGC CAGGCTGGTC TCAAACTCCT 1440
GACCTCAAGT GATCTGCCTG CCCTGGCCTC CCAAAATGCT GGGATTACAG GCGTGAGCCC 1500
CCACATCAGG CCTGTGGCCC GTTCTTCATC AGCTGCTGAA TGGTCCTCAG AGCTGAGAAA 1560
GTCCTGGGTT GGTTTTGGTG AGGAGTTACT GGTGTGGTGA GGTTCTGTCA GTCTATCTTC 1620
ATCATGGCCT TGAGGGAACC TAATGGTGAG 1650
|
