Tag | Content |
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EnhancerAtlas ID | HS139-35648 |
Organism | Homo sapiens |
Tissue/cell | Myotube |
Coordinate | chr22:39760300-39761620 |
Target genes | Number: 12 | Name | Ensembl ID |
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TF binding sites/motifs | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
EWSR1-FLI1 | MA0149.1 | chr22:39760661-39760679 | AGAAGGTAGGAAGGCAGG | + | 6.76 |
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| Number of super-enhancer constituents: 1 | ID | Coordinate | Tissue/cell |
SE_27409 | chr22:39759108-39761708 | Esophagus |
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| Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder | Number of disease enhancers: 2 | Chromosome | Start | End |
chr22 | 39760819 | 39761142 | chr22 | 39760725 | 39761343 |
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| Number: 1 | ID | Chromosome | Start | End |
GH22I039364 | chr22 | 39760819 | 39761142 |
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Enhancer Sequence | GGCAGGTTCC CCATCTGCTG TGGGTCAGCG AGAGGCAGGG CCTCTCTGAG CCTTAGCCTC 60 CCTGACTGTG AAATGCTCTA AGTATAAGAC TGCTTTGTGG GGATGATTTG CAGATTTTTA 120 TGGGGATTAA AATAGATGAT TTAGGTGCCT TCTTCCATTG GCACCAGCTC CTGGGAGGCT 180 GTGGGCTGGT TCAGGGTCTC AGAGTGGGGA CAGACTTGTA AATAGGTCCC AGCCAGGAGT 240 GACCAAGGCT CAGGGTGGGA AAGAGTGACT GGGAAGTGGG TTGTCCCTGA AGGTGTCTGG 300 GAGTCACTAT ATCCCAGCAG CGTTCAGAGG GCAAAGAGGA GTTCGCTCCC ATTGAAGATG 360 AAGAAGGTAG GAAGGCAGGT GCAGAGTTGT CAGACAGCCT GAGGACACCA CCCACTCTCA 420 GCCCTCTGTG GTGGCTGCAT AGGGTGGGGA GGGGGACAGA TGAGATCAGG GTAGGCCACA 480 AAGGGCTTGG TGCTTCTGGG GTCTCTGTTT CTATGTGTCT CTGAATCCAG TAGCCAAGGA 540 TCCTGAAATC CAAGATTCTG AGATTCCTTC TGATTTGTTT TTCTGAGTTT GACATAGATC 600 TCCACCAAGC GCCATCTGGA ATCCGTTTTT AAAAAAGACT CGGGATTGGA TTTTAAAGAG 660 GGCGGAAAAA AACCAAAGAG GCTTGGCAGG TTTACCTTGA TGCCTTTTTT TAGCGTTTGC 720 TTTAGCTCGA GGGAAGCTTG TTTTCCCTCT GCTTGCTGGT GACCTGGGTC CTCCCTTGGC 780 CATCACCCTC CATCCTCCCC TGTTTCTGGG CCTCTGGCTC TGCCTCTGAA GACCTGTCTC 840 CCTTCCCCAC AGCAGATCCG CTTGTTGGAT GAATTTTCCC CAGTGTCTCG GCTGCTGTGG 900 CCAGTGTGGA ATTTCATTCT GGTTTCATTT CCGGTTCTCC AGTGTCTCCT TGTGGCTGCT 960 CTGTGTGCCC CTTGCTGTCC CTGCAGATCT GGCCTTAGCA AGTGACTCAG GGATGCTGCC 1020 TGGCACAGGG CACCAGCTTT GGATCCAGAG AGACTCAGGT TCAAGCCTCA ACTCCACTCC 1080 TGCCCAGCTG CGAGACCTGT GCAGGTCCCT AGAAGCGGCT CTGAAATGGG AATAAGAATA 1140 TTGAGCTGGT GGAGTGAAGA GCATACATTT CTGGGCACAC AGCAGGCCCT GGGCAAGTCT 1200 CTGCTCCTCC TCCCATGTAC TGTGAGTGGC TGAGGGGCAG AAACCTGAGG CTTGTGTCGT 1260 GCTTTGGGGG AGCTCCCACT CAGGGTGGGG TACAGCTGCT AAATGGAGAA GTTAAACCCT 1320
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