Tag | Content |
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EnhancerAtlas ID | HS133-31051 |
Organism | Homo sapiens |
Tissue/cell | melanoma |
Coordinate | chr8:121868310-121870440 |
Target genes | |
SNPs | Number: 1 | ID | Chromosome | Position | Genome Version |
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TF binding sites/motifs | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
EWSR1-FLI1 | MA0149.1 | chr8:121870332-121870350 | GGAAGGGAGCAAGAAATG | + | 6.21 | Lhx3 | MA0135.1 | chr8:121868669-121868682 | TAATAATTAATTT | - | 6.25 |
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| Number of super-enhancer constituents: 1 | ID | Coordinate | Tissue/cell |
SE_35350 | chr8:121868803-121870452 | HepG2 |
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| Number: 1 | ID | Chromosome | Start | End |
GH08I120856 | chr8 | 121869042 | 121870511 |
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Enhancer Sequence | CTATGCCTAT AGAAATGACA TTGGGATCAA TTCAGAGATC GTATTTTTTT TTCTGGATTT 60 AGGAAAAGGA GAGATGTCTT AATGAAACAT GTCAAGTCTG ACATAATAAC CACTCTCAGA 120 TACCCACTGA GAATACTGAC TAAATGCCAT CAACTAAATT AAGTTCCTAC AGGACACTAG 180 AAGAGAAAAA TGAAACACAT TTATCTTAAG AAATACTATA GAATTTGAAT ATTTTCTAAA 240 GAGGTGATAA AATTAAAATG CAATTGTGCC TTATTTATGT GATAAATTAA GATTTGTAAT 300 GACATTTCTG TGGTTACAGT TTGTGACCTC ATTAAAATGT TTTAACATGA TATGTAAAAT 360 AATAATTAAT TTCTGAATCT AAATATTGTT TAAAGAGTTT GTTGACAATT CCAATTGCTT 420 ATTGCCTCAG AATTTCTCCT AATTGAAATT AATTTTTAAA AACTAAGAAC TACAATGACT 480 CAAGAGAAGT GTATGTAATT TGGCTTTACT CTCGGTAGCA CACAAATTAT GAGAGGCTCT 540 TTAACAACAT AGTTATGCAC TGAAATAAAT GAAAGAAAAT ATTTATGTGG ATGGAATATA 600 TAATAGTTAA AAATTTTTAT GTCTTTAGAA CTCATCCTAA CATTGACATC TTTCCAATAG 660 AACACCCCAA CTTGAATTAA ATTTCAGTTT TCATGTTTTC ATTGATATTA TGCTGGCTTC 720 CAGTCCTTTA AAATAAATGA TATTAGAAAT ATTTTCCAAA TTTTGTCATT ATGAAGGTAT 780 ACTTTTCAAG GAAGGACAAC AGAACATATT TCAATGAGCA GTGTGTTAGC TTGGTTTATT 840 CCTTTAAAAT ACATGGTAAA CTATTTAAAA TATGATAAAT GGGCCTCAAT TTGTCACCTT 900 TGGTCTAGGA ACGAAAAGAG TAGGCCTGAC CTGGGTATCC TTCTAGAGGA AGTAAACATT 960 ACTTTTTACA CAGGGTAGTT AGAGTCTCCT ATTTCTGGCC CTCAGGGAGT CCACTGAGAT 1020 GAATGCGTGG ATTCTAGTTC AACTTTACGG CTCGCTCACC ACAGCCACAT AGTCCCAGAC 1080 ATTTGAGAGT TGGAATTATT TAGAGAAGGG AAGACTGTGT TTGCAATGTG TTATACTGTA 1140 ATTTAGTGGA TACTGACCTG TCTCACAACA TCTCTACAAA TACAGAACAA GAGAAGGAGG 1200 GACCATTAAG CTGTGGTTTG AGGGATTTCA TTGACACACC AGGGAACATG TGTTTGGCAG 1260 CAGATTATTC TTAAACCTTG CAATGGTTGA TTGAGGAAAA TAGTGAGAGC CTCTGCCTTC 1320 TCTTCCTTTG GGCTACAGCT GGATTTCTCC AATATGAATG TAATGACCCA GGTGTAGTGT 1380 AGCCTTGTCT GAAAGCGGAG GAGTGGGGCA TACAATGATA TATAGTCCTT AGAGCTCTAG 1440 AAGGTTAGGA TTTCATGGCC TGCTGTTTAA TCATTACACA ATCAAACATA ACTGCAGCTC 1500 AAAGGCAGGA AATGAGTTTT ACCACAATTT CCAAGCAAGT AAGGAAATGG TCTGCATGGG 1560 CTGCAATGAA CTGTGCTCTT GCTGTTTTGC ATTCTTGCTG AATGCCTAAG GGAGCCCTCT 1620 CACGCATGGA CCTCTGGTAG AGGAGGAGGG GGGCTTTGAA TTCTGTTTTG CCAGTGACAC 1680 ACTCCATTGT ATATGACCAC TAAAAGGGCC AGACTGAATT ATGCTCATAC AGGATGAAGC 1740 TGCAACATGT TGTAGTAAGG AGCAGCTTCC TGAGTCATGT GTCCTAAGTG AAAGCCACCC 1800 TCATCCTGGG CTGACTGTCC ATCCCAGGCC CAGCCTGTAC CAGCAGTCAC AGGGGAGGGT 1860 CATTCATGGA GCAGTCTGCT TGAAAGGGCT CCTGGCTCAG GTTTCCCAAC AGCAGCTGCT 1920 TGTCATGTAG GCATGTGAAA CCTTTGAATA GAGTATGTGA GATGTCTGTC TGACTTACAA 1980 GAAAAGCTCT GCAGCTCTGA ACTCAGGGAA TGAAATGGCT TTGGAAGGGA GCAAGAAATG 2040 GCAGAGGCCA CTAGATAGAA GGAGCAGGCA TCTGTGGGCT GAGATAACAG AAAGAGGACC 2100 ACACTTTTTT TAATAGAACC ACTTCAAATT 2130
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