Tag | Content |
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EnhancerAtlas ID | HS178-16539 |
Organism | Homo sapiens |
Tissue/cell | Skeletal_muscle |
Coordinate | chr3:9037790-9039200 |
TF binding sites/motifs | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
EWSR1-FLI1 | MA0149.1 | chr3:9038234-9038252 | GGAGAGAAGGAAGGAGGG | + | 7.09 | EWSR1-FLI1 | MA0149.1 | chr3:9038242-9038260 | GGAAGGAGGGAAGGAGGT | + | 7.56 | EWSR1-FLI1 | MA0149.1 | chr3:9038238-9038256 | AGAAGGAAGGAGGGAAGG | + | 7.68 | ZNF263 | MA0528.1 | chr3:9038243-9038264 | GAAGGAGGGAAGGAGGTGGGG | + | 6.33 | ZNF263 | MA0528.1 | chr3:9038236-9038257 | AGAGAAGGAAGGAGGGAAGGA | + | 6.54 | ZNF263 | MA0528.1 | chr3:9038239-9038260 | GAAGGAAGGAGGGAAGGAGGT | + | 6.82 |
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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: 1 | ID | Chromosome | Start | End |
GH03I008996 | chr3 | 9037893 | 9039341 |
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Enhancer Sequence | TCATCTGTTA AATGGAAATG GTAATAAATA GAACCTATCT TACAGGGTTA TTAGAAGGAT 60 TAAGTGAGTG AATATACATG AAGTGCTTGC AACAGTGTCT GGCACATAGT ACCCTATAAG 120 AGTTACACAC ATGTTGTTAC CAGAGGCTGG TGCACTTCTA AGGGCCACGG ATGGCATGGA 180 AAAATCAAAG AGCAGGAGGA GGAAACTCCC TTGTTCACTC CCCATCACTC CCCACCACAC 240 ACATGCACCA GGGCTCCCCT CTGGAAGCAA CTGGCTCAAG AAGACCATGC TTGTGTCCCC 300 ATGAGATGCA GTGGCTTTGG GATGTATTTA GCTCTTAGTG ACTGAGGCAG CCTTCTGCAG 360 GGAGCAGGCC TCAAACAGTC AAGTCAGCTT CCCCAGCTAG CTACCCGACA AATGTCTTTA 420 AATGCTATTC TAACCTGGGT GTTGGGAGAG AAGGAAGGAG GGAAGGAGGT GGGGAAATGA 480 CAGCACCACT AAATGGGTCA GACTAACTCA GATCTTGACT CAGAGTCACA TTCTCAGTAA 540 AACAAACAGA GATCTTGGTC CCTCTCTCTG CAGCATCTTT GAATCTCACA TCCGGCCGTG 600 TGCTGGAACT GCCTGCTAGC CCATCTGCCT GCCTCGTTAC AAGAGTCAGA AAGGCCGGAG 660 GGTTTGCAAG GGCAGGAGCT GAGCCCAGAC AGCTGCGTGC TCCTGGGTTC GCCCAGGGAC 720 TTCCTCTGAC CCAGATTCCC CAAACTAAGA AAGGCGCTGA CCTAAGCAGA GGTTTTCTGA 780 TACTCAGAGG GGCACAGAGG GGCTGCCTCC GGTTTCTGCC TTTACCATCA CCAGAGCCTC 840 CAGCAGTCAC TGGACAGCAG CCTGAAGTTG AAAGAGTGGG GCAGCAGGGG GAGCAGACAA 900 TGTGAGGGAA AGAAAACAGG AGGAACAGGG CGAACCTCCA GCTCAGAGAA AGCACGTGTG 960 TTTGCAGACG TCGTTACATA AGTGTGTGTG GTGGAAACAG TAATAACAGC TCCCATTGAT 1020 TACTAAGTCT GTTATTTGGG CTTCTCGTGC CTGAAACAGA ATATGTTTCT CCCCCTCATC 1080 ACTCTCCCAC ACTCTGTTAC CCAAGCTTAC TTCATTCCCT CATCTTCCCC ATCTCAGGAA 1140 ACAGAACTGC TGTCTACCTG CTCACCCAGG CCAATGCCCT GGCATGGCTC TGCACACCTC 1200 ATCCATTAGC GACTCCTTCA GAGTGTCCCC TGGATCTGAC CATGGCTCAC CACCTCCCAT 1260 GCCACCCTCT TCACTTCCAT ACTTGCTTAG GTAGAGCCGC TTCTCCCCAC AGCAGCCTAG 1320 AGGGTCCTTT ACAATCATAC AATCACATCA TGAAACTCCC CTGTTCAAAA TCCTCAGAAG 1380 GCTTCCCATG GAGGCTGGAA CAAAATCCCA 1410
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