Tag | Content |
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EnhancerAtlas ID | HS139-29768 |
Organism | Homo sapiens |
Tissue/cell | Myotube |
Coordinate | chr2:109873320-109874790 |
TF binding sites/motifs | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
EWSR1-FLI1 | MA0149.1 | chr2:109873808-109873826 | GGAATGAAAGAAGGAGAG | + | 6.05 | EWSR1-FLI1 | MA0149.1 | chr2:109873775-109873793 | AGGAGGAATGAAGGAAAG | + | 6.1 | EWSR1-FLI1 | MA0149.1 | chr2:109873804-109873822 | GGAGGGAATGAAAGAAGG | + | 6.71 | EWSR1-FLI1 | MA0149.1 | chr2:109873874-109873892 | GGAAGGGAGGAAGGGACG | + | 6.74 | EWSR1-FLI1 | MA0149.1 | chr2:109873858-109873876 | GAAGGGAAGGAGGGAAGG | + | 6.84 | EWSR1-FLI1 | MA0149.1 | chr2:109873779-109873797 | GGAATGAAGGAAAGAAAG | + | 6.95 | EWSR1-FLI1 | MA0149.1 | chr2:109873866-109873884 | GGAGGGAAGGAAGGGAGG | + | 7.93 | EWSR1-FLI1 | MA0149.1 | chr2:109873870-109873888 | GGAAGGAAGGGAGGAAGG | + | 9.83 | EWSR1-FLI1 | MA0149.1 | chr2:109873862-109873880 | GGAAGGAGGGAAGGAAGG | + | 9.93 | ZNF263 | MA0528.1 | chr2:109873859-109873880 | AAGGGAAGGAGGGAAGGAAGG | + | 6.03 | ZNF263 | MA0528.1 | chr2:109873801-109873822 | TGAGGAGGGAATGAAAGAAGG | + | 6.06 | ZNF263 | MA0528.1 | chr2:109873876-109873897 | AAGGGAGGAAGGGACGGAGGG | + | 6.42 | ZNF263 | MA0528.1 | chr2:109873823-109873844 | GAGGGAGGGAGGGAGAGGAAG | + | 6.44 | ZNF263 | MA0528.1 | chr2:109873814-109873835 | AAAGAAGGAGAGGGAGGGAGG | + | 6.47 | ZNF263 | MA0528.1 | chr2:109873854-109873875 | AGAGGAAGGGAAGGAGGGAAG | + | 6.51 | ZNF263 | MA0528.1 | chr2:109873879-109873900 | GGAGGAAGGGACGGAGGGAGG | + | 6.53 | ZNF263 | MA0528.1 | chr2:109873842-109873863 | AGGGAAGGAGGGAGAGGAAGG | + | 6.56 | ZNF263 | MA0528.1 | chr2:109873773-109873794 | GAAGGAGGAATGAAGGAAAGA | + | 6.58 | ZNF263 | MA0528.1 | chr2:109873867-109873888 | GAGGGAAGGAAGGGAGGAAGG | + | 6.64 | ZNF263 | MA0528.1 | chr2:109873817-109873838 | GAAGGAGAGGGAGGGAGGGAG | + | 6.97 | ZNF263 | MA0528.1 | chr2:109873836-109873857 | AGAGGAAGGGAAGGAGGGAGA | + | 7.07 | ZNF263 | MA0528.1 | chr2:109873827-109873848 | GAGGGAGGGAGAGGAAGGGAA | + | 7.53 | ZNF263 | MA0528.1 | chr2:109873863-109873884 | GAAGGAGGGAAGGAAGGGAGG | + | 7.9 | ZNF263 | MA0528.1 | chr2:109873833-109873854 | GGGAGAGGAAGGGAAGGAGGG | + | 7 | ZNF263 | MA0528.1 | chr2:109873851-109873872 | GGGAGAGGAAGGGAAGGAGGG | + | 7 | ZNF263 | MA0528.1 | chr2:109873845-109873866 | GAAGGAGGGAGAGGAAGGGAA | + | 8.43 |
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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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| Number: 2 | ID | Chromosome | Start | End |
GH02I109257 | chr2 | 109874236 | 109874412 | GH02I109254 | chr2 | 109870692 | 109873502 |
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Enhancer Sequence | GACTAACCAT CAGCCTCTAC CTAATTGAAT GGCATTTTTA TGTGTTTTTC ATGAACGGTG 60 GTGGATGGAG ATGTGTGGAG GACTAGCAGC TCTTCATGCT GGAGGGAGTT ATTCCGCCTC 120 TGCTCTCAGA CAGCCTGTGA CCAGGCACGG GTCACATTGC TGCCCTGGAC TTGCACTGTA 180 TGGCATTTGA ATGTCATGTA GGGGCACCGT GTATTTCAGT GGCTGTGTCT AGGCAGCCCG 240 AAAGCCACTG AATCCCTCAT GTCCACTCTG CAGCCGACAT TCACTCAGCA TCCTGGAAAA 300 GTGCCCACTG GGGCAGGAGC TTCTCTTGCT CATGTGGACA TGACGGTAAG TCCTTCTTGG 360 AGAGGCAGCA TCAAGTCATG TTGTTCGTTC TGTGGCCAGG AGGTACAAAG TCAGCTGTTT 420 CTGCTTTTAA GTGATGTGGG CTTAAGGAAG AGGGAAGGAG GAATGAAGGA AAGAAAGGAA 480 TTGAGGAGGG AATGAAAGAA GGAGAGGGAG GGAGGGAGAG GAAGGGAAGG AGGGAGAGGA 540 AGGGAAGGAG GGAAGGAAGG GAGGAAGGGA CGGAGGGAGG GAGGAAGAAG CCCCATGGCT 600 TTCTTGTAAA TAGCAGCTGC CCTGAAGTCT GTGAAGGGCA CACCAAGAGT CTGGCTGGGA 660 GGTTGTCAGC TAGGAAACTG TGGCCCAAGT TCGTGGTGAG TGAGGAGTTA CTTTCTTCCC 720 TTGACCACTG GAGCAGGATA GACTCTGCCT GCCACCCATC CCATGAAGAA GACTTTCCTT 780 CTGAGTGCCT TGGTTTGCGC TTCAGGGAAG CCACTGACAC GTTCATTACC TGTTTCCTGA 840 AGTAGACAGT TAGAGCTCCC TGTCTCAGTG TCCAAAAAAA CCAAGGGGCC CCAAGTGCAG 900 AAACAAGGGC TGAAAATGTA TGTTTTACGG ACAGGAGACA GCCAGCCTGT TTAAGTGGAG 960 GCTTTTTTGG AAACCCCACT TTCCCAGTGA GTCACAGTAA ACACAGACAG AGCACACTGC 1020 TTCTCTGACA CCAGGGCCAG GGCTGTCCTG GGCTCAGAAT GAATTAGACC AGCTTGCCTT 1080 TTGTGTTCAC CATTCTAGCA TTTCTTTCCC TGCTTGATTG TCACCACATG TGCACACACA 1140 TACCCACATA CCTGTGCACA CATGTACACT TTCTTATTTG CTGACCCTCA CAGCCCTGCC 1200 ATCCCTGGGC TACCAGGCAG ACTTTCTGAT CTGGAGCTTA ACCGGCCCAG ACATTGGAAA 1260 CACCAAGCAA CTGGTAGCTG GTAAGACTTT TACCCCATCA ACGAGGCTTA CGAAAGAGTA 1320 AACTTACCTT AATAATGCCT AGTGGCCAGG TTTCCAGGAG TGGGGGACAG CCTGGCGCTG 1380 TTTGTAGGGG CTGAAGGGAA TGTTTACTGA GGGGATCCTG ATGCAGTGGC CGCTGTGACA 1440 GCCAGTCAGG AGGTCTTGTC CCCATTCTAA 1470
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