Tag | Content |
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EnhancerAtlas ID | HS133-04969 |
Organism | Homo sapiens |
Tissue/cell | melanoma |
Coordinate | chr10:114394010-114395350 |
Target genes | |
TF binding sites/motifs | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
FOSL1 | MA0477.1 | chr10:114394020-114394031 | GGTGACTCATC | + | 6.32 | FOSL2 | MA0478.1 | chr10:114394019-114394030 | GGGTGACTCAT | + | 6.14 | JUN(var.2) | MA0489.1 | chr10:114394021-114394035 | GTGACTCATCTCTT | - | 6.17 | JUNB | MA0490.1 | chr10:114394019-114394030 | GGGTGACTCAT | + | 6.32 | JUND | MA0491.1 | chr10:114394020-114394031 | GGTGACTCATC | + | 6.62 | Nr2f6 | MA0677.1 | chr10:114395153-114395167 | AGGGTCAAAGCTCA | + | 6.09 | POU4F2 | MA0683.1 | chr10:114394666-114394682 | ATGCATAATAAATAAA | + | 6.42 | Rxra | MA0512.2 | chr10:114395153-114395167 | AGGGTCAAAGCTCA | + | 6.15 |
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| Number: 1 | ID | Chromosome | Start | End |
GH10I112634 | chr10 | 114393966 | 114394745 |
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Enhancer Sequence | AGACCCTCTG GGTGACTCAT CTCTTTTGAG ATCCTGATTG TCCATTTTTT GGTTGGTGTT 60 CTGGCAGCAG TGTGTGTTGC CCTGAAGGCA CCCTCTCATA TGGTGTTGAC TACACTATGC 120 TGTGCTATTT AATTCTTGTT TTGGATTGTG CCTCGAGTTT TAAGTCACTT GACAATACAG 180 AAGGTTTCTT TCTCCAAAGA TTATCAATAT CATACCATTG CCTCTCGGTG GTTATACACA 240 CACACACAGA CACACACACA CATACACACA CACACACACA CACACACACA CACACACGAA 300 TTTCATGTTT TCTTCCTTTT GAAACTAAAT GTGATCTGTC TGACCTTTCT GAGGAGTCTG 360 CTGCTTTTTC AGATTTATGT CCCTGTGACA AGGTGGTTTG GCAAGCTGTT TGTCTTAATC 420 ACTCAGCATC TCCATTAGAC AAGCTGTTTA AAAATCTTCT ACGTAATTAT CTTTTTTGAC 480 TCTCACTCTT CCACATTCTT TTCTTTATTG TAAACTTTCT TATGACTTTT TTATATATCT 540 GCCATGTTCT AAAAGGCATT TAAGCCTTCT TACACTGTTT TGTCTGCTTT TCATTAAGTT 600 TGCCATCAAT TTACAATCCA TGCCCATTGC CTCCTTCACA ATCTGAATAC ATAAACATGC 660 ATAATAAATA AACTCTGGGG TTGAATCCTG GACTGAGTGG CCAACATTTT TTCTGTGTCT 720 TCCTTAACTG TTAAAATAGG CAGACAGAGG AGCATTAGAG GAGCTAATTC TAGGAGTCTC 780 CTACGGACAT TTGCCGGAGT TTTCACTGCC TTGTTGTTGC CTGTAACTGC AAAGTTCAGA 840 AAGCTGGGGC TGGAGGTGCC TTTATTCATA ATATGAGCCA GGCACTGTGC TCATTATTTG 900 GGGGGAATAA AAGATAACAC ATTTCCTGCC TTCAAGCAGC TTTTACTCTG GTAAAGAGGA 960 TAATGCAGGC ATGTAAATCT TGTGGAGATG AGACAGCGTG CTGAGGAATT TAAGGAGAAA 1020 GATCCCTTTG GTAAAGGCAG ATGCAGAATT CATGGCAGAT GTAGTGTTTT AGCAGAACCG 1080 TGAGCAGTCA GCAGGATTGT ACGGATTGGA GATTGGTAGA GGCATTCCAG ACAGGGAACC 1140 GCAAGGGTCA AAGCTCAGAG GTGGCCAAGT CTAGAATATA TGCCAGAGAG AATTGAGAGA 1200 GAAGCCTGAA AGAGTATTTA GGCCTAAATT CTGAAAGGTT CTAAATGCTG GCTTAAACCT 1260 TGGATTTTTC TTGGTGAGCA TGGCCAGAGT GGTGTTTTAG GAAGATTTTA GAAAGATCAA 1320 ACAATCGAGA CGTACTGATG 1340
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