Tag | Content |
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EnhancerAtlas ID | HS133-05003 |
Organism | Homo sapiens |
Tissue/cell | melanoma |
Coordinate | chr10:120718080-120720410 |
Target genes | |
TF binding sites/motifs | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
EWSR1-FLI1 | MA0149.1 | chr10:120719002-120719020 | GGAAGGGAGGAGGGATGG | + | 6.85 | NFE2L1 | MA0089.2 | chr10:120718770-120718785 | AATGCTGAGTCATTC | - | 7.82 | Nfe2l2 | MA0150.2 | chr10:120718772-120718787 | TGCTGAGTCATTCAC | - | 6.55 | RREB1 | MA0073.1 | chr10:120718656-120718676 | TCCCCAGCCACCCCCCACCA | + | 6.27 | RREB1 | MA0073.1 | chr10:120718666-120718686 | CCCCCCACCACCCCCCATAC | + | 6.73 | RREB1 | MA0073.1 | chr10:120718663-120718683 | CCACCCCCCACCACCCCCCA | + | 7.01 | Stat4 | MA0518.1 | chr10:120719871-120719885 | CTTCCAGGAAAGGG | + | 7.25 |
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| Number: 1 | ID | Chromosome | Start | End |
GH10I118958 | chr10 | 120718221 | 120721823 |
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Enhancer Sequence | ACACTCCAGC CTGAGAGACA CGGTGAGACT CCTTCTAAAA AAAAAAAACA AAAAACTCTT 60 TTCTTATAAA TGACCTAGTC TCAGGTATGT ATTTGTAGCA ATTCGAGAAC AGACTAATAC 120 AGTGGTCAAG TAATCAGGGA ACAGTTGAAC AGTTTCTTGC ACGACTTCTC AGGGCCTTTA 180 ACATGCTAGT GTGTCTTGTG AATACCCATG AGCGGATACA GGAATGGTTG TCCTACTTCT 240 ATTTTTTTGT TTTTTTAGTT TTGATTTTTT ATTTTGTCCT AAATTTATGT AACCACAGAA 300 GCCTCTTCTC AGAGCCTCTG GTGGGATTTG CCTCTGTAGA GTGGAGCTGG GAAAATCCTG 360 CAAGAGCGAG TCCAGTGGTA ACAGAGGAAA AGGCCCATGT TCAGGGAGTT TGGAGCTCCC 420 CATATGGAAG ATGCATTTGC CTCCCTGTGG GATAACCTCA GGGCCACTTT AGGTTCATGG 480 GGCTGCAAGC TGGTGCTCTA CAGATCTGCA GCAAGAGTGT GACTTCCAGT CCTGTGTTGC 540 ACTGAATTCC AGGGACCGCG TGTGTCCCCG TTCCCCTCCC CAGCCACCCC CCACCACCCC 600 CCATACACAT AGTTGGCATT TAACCTTGCC AAATATCTTT GGTATGGCAA TAGAATGATC 660 TGGCTCCTAA AGAAAGAAGT CAGAGTTCAA AATGCTGAGT CATTCACCAC GAGAGCAGTG 720 CCTGAGGAGA AGTAGGTCAG CCTGGGCCGA GCCTCCCCAC CCCTCCTTGG CATCAAAAGC 780 ACCCAGCACA GTAAAGGCAG CTCACACATG GCCGGGGCTG TTCTACAGGC TCTATCTGTA 840 TCCACTCTTT AAAGCCTCAT GACAATGCTA CAAGGGGTAA CTGTGAGTCT CCTGAAATTC 900 CAGATAGGAA ACTGAGGCAC AAGGAAGGGA GGAGGGATGG ACCCCCAGCA ACCCGGCCAC 960 ATCCCTAACC AGAAACAAAG GATGGATCAT CCTAGACACT GCAGCAAAAG ACAAGAGTTA 1020 ACCACTCATT CCCCAAACAC AGGAGCAGAC CCCACCCTTG AGAAGCTTGC ACTGATGGAG 1080 ACAGACAAGC AGCACCCCCA CGGCAACAGC AGTGGGCAAC AACCTGCTAG GAGGAGGCCC 1140 GATGCCATGG GAGTACCAGT AGGGGTACCC CGCCTGGACT TTGGAGGTGG TGGTACTCAG 1200 GGAGAGCTTC CTGGAGGAGG CAGTCTCTAA GCCAGGTTCT GAGAACAAGT GGGAGTTAGC 1260 CAGGTGAAGT AACTTTAACA TGCTAGTGTG CCTTGTGAAT ACCCATGAGA GGATACAGGA 1320 GTGGTTGTTT CAGCCCAAGG ATGCACCTGT GCAGAAACTT AGAAGCCAGG AGACAGCAAG 1380 GGCCTTTTGG GGAACTTGGG GAGGAACAGA GTAAGAAGCC GAAGCCAGCT GCCATCAAGG 1440 AAGCTCTCTG ACCCACAGCC ACGCTGTAAG TTGGAAAGTC TGGATTCAAA TCCTGACTCC 1500 ATTTATTCCT AGCTGAGTGA CCGTGGGCTG TTAAACAACC TTTCTGGGCC TCAGCTTCCA 1560 TATCTGGAAA ATGCAGAAAG GAACAGTACC TTCCACACAG GGCTGTTGTG TGGGTGAAAG 1620 GATCTGCTGT GTATCAAGCA CTTGGCCTAG GCATAAGGAA GCACTAAGTG GTGTCCACAT 1680 CGTCATTGGG TAGGAGTCAG CCCAAGCCCT CCAGCAATTC AGCAAGAGTT ACACAAAGTT 1740 ACATTCAGTC CTGCAGAGCA GGTCCAGCTA AGTACAAAGG CAGGCTTGGG GCTTCCAGGA 1800 AAGGGGAGAA GCAGCCGGTG AGACCACAGG AACATCCGCC CTCCCCGCCC TGGCCCCAGG 1860 CCTCCGGGTT GCCTCCTCCT TCCCAAGGTA AGGCCCTGCC AAGAAATTCC ACTGAAATTC 1920 CAAGAAAGTT CACTTTGAGT TTCACCCAGT CCCTAAATGG AAACACGCAT GCGCACGTGC 1980 ACACACACAT GTGCACACGC ACACACAGCA TGAGGGGAAA CCTAGAGCAT CTTTATTTTA 2040 TCCCCACCAT GAAGCGGACT GGTTTGGAAA AGTACCCTGC CTGCCTCTTC ATGGGGCTGG 2100 GTGTGGTCCT GAGCAAGATG GCAGGAGGTG GACGTGAAAC CCATCTCTTC CCCCGCCGTG 2160 GGGACATCAT TTCTCATTGG GAGTTGGCAG AAGGAGCTGT GATAAGGGGC GTCCTCTCTC 2220 CAAGCCTTGG GGATCTGGAA GGGATGCAGG TGATTCCACC CATAAAAAGC ATCCTGGCAG 2280 ATCCCCAAGC TGGGCCACCT GCATCTGCAG CATTTCTCAT GAGGCCTCCT 2330
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