Tag | Content |
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EnhancerAtlas ID | HS193-05126 |
Organism | Homo sapiens |
Tissue/cell | U87 |
Coordinate | chr10:101520280-101521810 |
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 | chr10:101521747-101521765 | AGAAGGAAAGAGGGAAGG | + | 6.46 | TFAP2A | MA0003.3 | chr10:101521245-101521256 | TGCCTGAGGCT | - | 6.32 |
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| Number of super-enhancer constituents: 1 | ID | Coordinate | Tissue/cell |
SE_34343 | chr10:101517664-101522120 | HCT-116 |
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| Number: 1 | ID | Chromosome | Start | End |
GH10I099761 | chr10 | 101521261 | 101521410 |
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Enhancer Sequence | AGAGAGGCTG GAGCCAGAAG AGCTGGGATG CAGGGAGCAG CATCCTGAGG CAGGAGCCAC 60 ACAGCAGCAG CACCTGGGAT TGTCCCTCAA ACTATTCCAT CCTCCTAGGC CTCTAGGCCT 120 TTGATAAGAG GGGTAGCCTT GAAGATTTCT GAAATGGCTT CATAGCCTTT TTCTCATTGT 180 TCTGACACCT GGCTCCCTTT TATCATTGCT AATCTCTCTA GCAAGTGATT GGACTCGGCT 240 AATCCAATAT TCTTGGATTC CTCTCCTGAA AATGCCCTTT CCTTCTCTAC CACACGGCCA 300 GGCTTCAAAT TCGCTAAATT TTTATTCTCT GCTTTTAAGT TCTGACTTTA GGTCATTCCT 360 TTGTTCACAT ATTTGATTGT AGGTTGTTAG AAGCAGCCAC ACTTTGTTTT TTTTGGAGAC 420 AGGGTCTTGC TCTGTCACCC AGGCTGGAGC AGTGGCAGGA TTATGACTCA CTGCAGCCTT 480 GATCTCCTGG GATGAAATGA TCCTCCCACC TCAGCCTCCC AGTAGCTGGA ACTACAGGCA 540 CATACCACCA CACCCAGCTA ATTAAAGAAA AAAAAATGTA AAGTTGGAGG ACTCACTGTG 600 TTGCCTAGGC TGGTCTCAAA CTCCTGGGCT CAAATGATCC TCCTGCCTCA GCCTCCCAAA 660 GTGCTGGGAT TACAGGCATG AGCCACCATG CCTGGCCTCA CCACTTATTG AACGCTTTGC 720 TGCTTAGAAA GGCGTGGCCT TTACTGTCTG TATTTCTGTC AGCACTTTGG CCACAACCGC 780 TCACACAGTC TAATAAATCC CAAACTTTCC CTTATCTTCC TGTTTTCTTC TGAGCCTTCT 840 AAACTCTTCC AACTTTTGCC CATTACCCAG TTCCAAAGCC ACTTCCACAT TTTCAAGTAT 900 CTTTATAGCA ACCACCCTCT CCTTGGTACC AGTTGTCTTC CTTAGTTCAT TTGTGTTGCT 960 ATAAATGCCT GAGGCTTTGT AACTTGAAAA GAAATTTTAT TTGGCTCACA GTTCTGCAGC 1020 CTGTACAAGA AGCCTGGTGC CAGTATATCC TAACCACAAC ATCATTGATT GGACCAATCC 1080 AGAAAAAGGG TTCTGATTGT CCAGGCCCTC TTGTACAGTC AAAAGACTGG CAGCTGGTGT 1140 TTATCTTTTC CTTTGAAGGC TCAGGGGTTA GCTGCTATAT AGACAAGGGC TGTCCTAATA 1200 ATAAACCTGA CTGCATTTGC ACAAAACAGT AGAGTTAGCT TTTCCCTTTC TGCCTTAAAT 1260 CTTGATGCTC GATTCTCTTC CTTACTAATG TGTTTTGTGG CATTTTTTCC TTACTGATAA 1320 ATGTGTTTTG TGGCATTTTT TTGTGGCAAA CTGATGCAGA CAGAAAACCA AATACCCCAT 1380 GTTCTCACTT ATAAGTGGGA GCGAAACATT GGCTACATAT GGACAAAGAC GGGAGCAATA 1440 GACACTGAGG ACTACTAGAG TGGGGAGAGA AGGAAAGAGG GAAGGGCTGA AAAACTACCT 1500 ATTGGGTACT ATGCCAACTA CCTGGGTGAT 1530
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