Tag | Content |
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EnhancerAtlas ID | HS098-29569 |
Organism | Homo sapiens |
Tissue/cell | HSMM |
Coordinate | chr2:37603660-37606020 |
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 | chr2:37605793-37605811 | GGAATGAAGGCAGGGAGG | + | 6.93 |
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| Number of super-enhancer constituents: 2 | ID | Coordinate | Tissue/cell |
SE_43498 | chr2:37600389-37607594 | MM1S | SE_67144 | chr2:37600389-37607594 | MM1S |
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| Number: 1 | ID | Chromosome | Start | End |
GH02I037375 | chr2 | 37603020 | 37606330 |
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Enhancer Sequence | TTTCACTCTC AGTTTCAGGG CCACTTTTTA CGTAGCCTGA AATTCTAAAA GTAGTTTTGA 60 AGTGGTTTAA CTGCCTCACC TTACTTCCCT TTTGTCTATC GCCTCTGTGT CTTTTATGGT 120 ACATCTTTTC CATCCCTCAA GTAGTGAAAT TACTGCTTTG TTGCAAGGGG CAGATAGCAT 180 TGTGTAAAGC TACTGCTGTG TTCCAAGGGG CTGAGGTGGA GAGAAAAGGT TGTTAGGTGG 240 TTGAGCCAGT AGGGTGGCAT AGGATACCCC TCAAATGCTC CTACACATGA ACATTGGCCC 300 CAGGCTCCTG GCAAGACATC CAGCAGCAAT AATTTATGAC AGTTTTATAG AGAGCTGGGA 360 TGAAAGGACT GTCTTGTGTC ATGGCTGTAT TCCTCAGCCG GAATTTGGTT GGCGTACGCA 420 CGCAATGTGA AGTCATCTTA TTGTGCTCAT ATTTCAAAGG CAACACATGG AACAGTGCCC 480 ACTCTCCTGA CATATCTGAA TTTGCCAGCG AAGAGTTTAG ACCGTTTGTT TGAGCATTAA 540 CATTAAGAGC ACAAAATTGC CAAGAAGGGA AAACAGCATG GCTTAAAGCA AACAAAACAA 600 AACAAAACAA AAAACCCCTA AATTCACAAA GGTTACAAAG GTAATATGAA AATAGATTTA 660 AAAACTCATA AATTATCAAC AGCACTGGAA ACTTTATTCT CTTACACTTA CTGAGCACTG 720 TGTGGTACAG GAGGTCCTTG GCACTCATGG ATTTAACATT TGTGGTTTTG GTTAACAAAG 780 AATGACATGT AGTAAGTGAC ATGAGCTAAG AGTTTGGCGT GGAGAAGTAA ACGAGCATAG 840 CTGACTACGA GCCACCAGTT TCACTGTTGT TCTCTAGTCA TCCTTGCAGT AACACTTGGG 900 AAGTGATAAA CCCCATTTCT TTGTAAAAAT GAAGCCCTCC TCCAAGCCAG CTGCTTTTTC 960 TGGAGATGTT ATTGAGAGGT CTAGAAAAAT GCTGGCTACA GTGAGTAGCT TTATAAGTGA 1020 TTTTAATCCT TTACAAATAG ATAAATTAAT GCTAGGAAAA GATAACTTTA AAACTTCAGT 1080 TTTAAAACTT TATTTAATGA GGAAAATTGT AAGCAACAAT GGTATTCAAA AGCACTTAGG 1140 ATATTTTCCT CGAGAATGTT AAAGCTCCAT TTTAGGTTAT GTTAGAATGA TTCCGTATCA 1200 AGTAACTGAT TGTGATCATC CTTTCATAGG TTTACCCATA GAGCTGTATA TTAGCATCCT 1260 CATTTTACAA ATAAGTGAAC ACAGAGTTTA AATTATTCTC AGTTGATGCT AAGACTAGAC 1320 TCTAGGGAAC TTAATTTCTC ATACATGACA TGGCTGATTT CAGCTCGATT AGAGGGGACC 1380 TTAGAGATTT TCTACTTCAC TGGCTTACTG GTTTTCAGCT ACACCCAGGG GGCATTTGAA 1440 AATATGTGGT GTGTGTGTGT GTGTGTGTGT GTGTGTGTGT GTGTATGCCT TTCTGTGCTT 1500 ATGTAGTGGA ATGGGTGGTG AATGTTTGTC ATGAAGACTG AGGGGTGCTT CTGGAATTTA 1560 GTGGTTAGGG GCAAAAATGA ATGTTCAGGA CTGTTTGCAC ACTAGAGAAT TGTCTCACCC 1620 CAAAAGCCAA TGGTGCCTCC ACAGCACTGA GTAGTTTTCA ACATTCTCAT TTTAAAGGTT 1680 TAGCTATCAA GATCCAGAGA GGATGGATCA CTTAAGATTC CATTGGTTTG CAAGTGACAG 1740 AAAATTCAAA CTTACCTGAG CAAAAAACGA AATTTATTTC ATGTCTCTGA CTTCAGACAC 1800 AGTTGACCCC AGAACCCTGT CTCTTGTCTA TCTGCTCTGC CCTCCTCTGG GTAGGCATTA 1860 AACTTAGGGA AGTACTTCCT TCTGGGGCAA GATGGCTGTT AGTAGCCCCA GGTTCATACT 1920 CCCATCACTC CAGTTTCAGT GCAAGGTGAG TACCTGTCCT CTGAGCAACA GTTCCACAAA 1980 GTCCTTGGCC TGACTGCCAT TGGCCCAAGT GGAGCTCTGG GACCTTTGCT GATTCAGTCT 2040 CTGGGCTGGT GGATGGAATG CACTGATTGA CTTTGGCCTG TGGCTCACGC CCCTCCCTAT 2100 AGCTGGGAGA AGTGTCAGCT TCACCAAACC ACAGGAATGA AGGCAGGGAG GAGGCGGTTG 2160 TCCAAAGGAA GATCTAGAAA AAGAGTGCCG TACAAGCAAG AGCAACAAAC GTCCATTACA 2220 GTAGGTAAGC GAGTTGGGTG ACGTATGTAC GATCCTAAGG CATGGTACCA CATTGCCTTT 2280 CTTTTTTTCT TTTTATTTTT TTTGAGATGG AGTCTCGCTC TGTTGTCCAG GCTGGAGTGC 2340 AGTGGCATGA TCTTGGCTCA 2360
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