| Tag | Content |
|---|
EnhancerAtlas ID | HS133-10013 |
Organism | Homo sapiens |
Tissue/cell | melanoma |
Coordinate | chr15:47675370-47676980 |
Target genes | |
SNPs | | Number: 2 | ID | Chromosome | Position | Genome Version |
|
TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| FOS | MA0476.1 | chr15:47676695-47676706 | TGTGACTCATT | + | 6.62 | | SREBF2 | MA0596.1 | chr15:47675869-47675879 | ATCACCCCAT | - | 6.02 |
|
| | Number: 1 | ID | Chromosome | Start | End |
| GH15I047383 | chr15 | 47675357 | 47677270 |
|
Enhancer Sequence | TAAGCTGATC CTCTATTTCC AAGGACATAG TAGATTGTGA TTCCCTATGG TCGAGGAGGT 60
ATGATCCTGG TTTCTTCATG CCTCAGCTCG TCTGGGAAGA GTTGTGGGCA AAGGTTTCTA 120
GCAGAGCTTC TGATTCATCT TGATAATTCA TTAACTCAGA TGGCACATAT GGAAAGTACA 180
GGAGGATGTG AGACGATAGT GCCTCCCATG ACGAGGGAAG ATGGGCACAA GCACTATGAT 240
TGGTCTCTAA CTCCTATGCC CTGGCTCATA GTTGATTTTG AAACCGGCCA GTGCTGGCCT 300
TCCTCAAGGG GTCATACTCT TTCACTTTGA GATCAGGCTT CTGGTATTTC CACATGTGGC 360
ACTGCCAGGG GCCTGGTACA ACACAGTAGT AGTAGTAGTA ATAATAATTT ATTGATTGTT 420
TTCTATGGGT CAGGCAATGA GCTATATGCT TTACCAGTTT TAACTCATAA GGCATAAGGA 480
CCCTGAGTTA AATATTAAAA TCACCCCATT TTGTAAGATA ATAAAAATTG AAGCTTTGAG 540
GTTAGCTAAT GCCCAGATTG AAGCTAGAGA GGTCAGCTAG TGGCCCAGAT TGACATATCA 600
AGGAATAAGA CTGGCACTCA GACTCTGCTA TGTCTGATTC CAGATGCAGG TCTCTAGCAT 660
GCTGAGAAAT TTTAGCACAC ATTCAATTTC TCATAACAAT TGTTCATTGT TCTCAAAAGC 720
ATCTCTGTAT ATCTCATGAC CCAAATTCAA GCTCCTGCTT CCACAAAGCA CATGCACATA 780
TATACAGATT CACACACATA GAGTGTTTTT CCACGATCTC ATTTACAATG GGCTCCGTTA 840
TTGCTTATAC CCAGTTTAAT TTTTGGCTGG GCCTTTAAAT ACTTTTTAAA TGTTAAGAAT 900
TCCAGGGACC TTCACAAAGA CCAAAGTAGC AGGGTTTAAG TTTTCCCACA AATCAGAATA 960
GGCAACTGCC AGCTTTCACA CGAGGTCCTC CCAACCCAGT GACAACAGTT GTATTAAAGG 1020
AATAGAAAAG CCCAAACATT GTATGCATGT TTAGTAGTGC ATAAGAGCTA CTTTAAAACA 1080
GATTTGGAAA AAAAGGGCAA ATTCAAAATA TTTGCTGCAT TTCTAGCGCC TATTCACTAG 1140
GCAGTCTCAT GTTGTTTTGA GCTCAGAAGC TTGGTTCTTT CCCCACTTCA CCTTTCTCTT 1200
TTCCCTGAAA CATCTTTATC TGCTTCCCAC TCTTCCATCT GTCAGAAGTT CCTGTTTGCC 1260
TTTGAAAGGA TTTCTCGGCA AGCTGACCTC TGTGGATTTC ATCAGCCCTG CATGCTTGCA 1320
CATGCTGTGA CTCATTTTCA CTAATCTGTG CAATGAGCAG TGAGCAGGGG CCAGCAGAGG 1380
CCCTGCAGCC TGCAAAGGAC TAATCAGCTA CCAACTGTGG CATATGAGGA TGTCTGAGTG 1440
GAGAGCTCCA AACGCCTACA CGCCTCATGC CCAGAAGCTC CTCCTTCTGT GTCCCCCACC 1500
CTTATTTTTT GCTCTTGAAT AAGAGGCATG AAAGCAAACA TCTCTAGCCC GGAGTAAGGC 1560
TCACACTGCC AAAACCATAT AGAGGAGTGT GTAGTTATTT TCCCATTTAT 1610
|
