Tag | Content |
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EnhancerAtlas ID | HS139-18136 |
Organism | Homo sapiens |
Tissue/cell | Myotube |
Coordinate | chr15:40269050-40270270 |
Target genes | |
TF binding sites/motifs | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
BCL6B | MA0731.1 | chr15:40270194-40270211 | TGCTTTCTAGTATTTAA | + | 6.66 | EWSR1-FLI1 | MA0149.1 | chr15:40269140-40269158 | CTTTCCTTCTTTTCTTTC | - | 6.34 | EWSR1-FLI1 | MA0149.1 | chr15:40269136-40269154 | CCTTCTTTCCTTCTTTTC | - | 6.84 | EWSR1-FLI1 | MA0149.1 | chr15:40269124-40269142 | ATTTCCTTCCTTCCTTCT | - | 7.43 | EWSR1-FLI1 | MA0149.1 | chr15:40269132-40269150 | CCTTCCTTCTTTCCTTCT | - | 7.69 | EWSR1-FLI1 | MA0149.1 | chr15:40269128-40269146 | CCTTCCTTCCTTCTTTCC | - | 9.47 |
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| Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder | Number of disease enhancers: 1 | Chromosome | Start | End |
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Enhancer Sequence | CGCACGGCGC GGACCAGCTG CCTCTGATGC GCCCCCTAGT TTCCTTTCTT TATTTTTTTT 60 TCCTTTTTCC TTTCATTTCC TTCCTTCCTT CTTTCCTTCT TTTCTTTCTT TCCTTTTTTG 120 AGATAGGGTC TTGCTCTGTC ACCCAGGCTG GAGGTCAGTG GCGCGTCCTT GGCTGCAACA 180 TCCGCCTCCC GGGCCAGCGA ATGCCCCCCA ACATTAATCC CCACCAAGTC CAAGCCAGGG 240 AAAAGGGGAT TCATTTAGAA ATCCAGACGT GTTGACCATG TTTAAAAACA AAAACAAAAA 300 CAAAACAAAA CCACCACTTT TAGAGAGTAA CCAAATGCAA TCTAAAGGAG CGGTCCCCAG 360 CGTTTTTAGG CACCAGGGAC TGGTTTCATA GAAGACAATT TTTCCACAGA CGGGTGTTAG 420 GGAAATAGTT TCGGGATGAA ACTGTTCCAC CTTACATCAT CAGGCATTAG AGTCTCATAA 480 TGACTGCTGA AAAAGCGCAC AACCTGGATC CCTCGTGTGC ACAGTTCACA ATAGTGTTTG 540 CGCTCCTATG AGAATCTAAT GCGGCTGCTG ATCTGACAGG AGGTGGAGCT CAGGCCTTAA 600 TGCTTGCTCA CCTCCGGCTG TGCGGCCCTA ACAGGCAGTG GACCTGTACC TGTCCATGGC 660 CTGGAGGTTT GGGACCCCTA ATCTAAAGGA TTTTTTTTCC CGCTATTTTC AAAAGATCTC 720 CAAAATCCAA GCCATGGAAA AAGGAAAATT CAATACCTCA TCTTATACAT TGAATAGAAT 780 TTCTCATAGG ACATTCCTTT GGATAAGGGC TTGCAACCCT GTGAAACATT TAAGAACTAA 840 TTTGGAGTCT TGATACAGTG CCAACTGCAG CCCCCAAAGG TACCAAACCA ATAATTATGA 900 TCCTAAATTT TATGCTTCTC AGAATCCACC CTGGATGTTT ACTTTCATGA TTTTGTTTTA 960 TTTTATCCAA GTGGATACAG TTTATGATTA CTCTTCACTA TTAAATTTTT TGAGGAAACT 1020 TAATCTGGCT AATTTTTATT AAATCAAGGG TTCTGTGTTT TGCATAATAG CAAGTACAAA 1080 TCAGCACAGT GTAGAGTATA CATTGATGCC TGTGGGCTCA TGGTGTGATG TCTGTAGCCT 1140 CTTGTGCTTT CTAGTATTTA AAAATGTCCA TGTTTATAAT GATAATAGGG ATTTCTGTTC 1200 CTTTAGTATT TCTGTTTCCC 1220
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