Tag | Content |
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EnhancerAtlas ID | HS068-05358 |
Organism | Homo sapiens |
Tissue/cell | GM18526 |
Coordinate | chr8:11361320-11362630 |
SNPs | Number: 2 | 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 | chr8:11361859-11361877 | GGAAGGAAGGAAGGAAGA | + | 10.05 | EWSR1-FLI1 | MA0149.1 | chr8:11361851-11361869 | GGAAGGAAGGAAGGAAGG | + | 10.83 | EWSR1-FLI1 | MA0149.1 | chr8:11361855-11361873 | GGAAGGAAGGAAGGAAGG | + | 10.83 | EWSR1-FLI1 | MA0149.1 | chr8:11361867-11361885 | GGAAGGAAGAAAGAAAAG | + | 6.98 | EWSR1-FLI1 | MA0149.1 | chr8:11361863-11361881 | GGAAGGAAGGAAGAAAGA | + | 8.26 | EWSR1-FLI1 | MA0149.1 | chr8:11361839-11361857 | GAAAGGAAGGGAGGAAGG | + | 8.62 | EWSR1-FLI1 | MA0149.1 | chr8:11361847-11361865 | GGGAGGAAGGAAGGAAGG | + | 9.47 | EWSR1-FLI1 | MA0149.1 | chr8:11361843-11361861 | GGAAGGGAGGAAGGAAGG | + | 9.6 | KLF13 | MA0657.1 | chr8:11361955-11361973 | AAGCCACACCCCTTTGTG | + | 6.56 | TP53 | MA0106.3 | chr8:11362559-11362577 | CACATGCACAGACATGTA | - | 6.19 | TP53 | MA0106.3 | chr8:11362559-11362577 | CACATGCACAGACATGTA | + | 6.22 | ZNF263 | MA0528.1 | chr8:11361845-11361866 | AAGGGAGGAAGGAAGGAAGGA | + | 6.28 | ZNF263 | MA0528.1 | chr8:11361840-11361861 | AAAGGAAGGGAGGAAGGAAGG | + | 6.31 | ZNF263 | MA0528.1 | chr8:11361860-11361881 | GAAGGAAGGAAGGAAGAAAGA | + | 6.36 | ZNF263 | MA0528.1 | chr8:11361852-11361873 | GAAGGAAGGAAGGAAGGAAGG | + | 6.94 | ZNF263 | MA0528.1 | chr8:11361856-11361877 | GAAGGAAGGAAGGAAGGAAGA | + | 7.03 | ZNF263 | MA0528.1 | chr8:11361848-11361869 | GGAGGAAGGAAGGAAGGAAGG | + | 7.42 |
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| Number of super-enhancer constituents: 7 | ID | Coordinate | Tissue/cell |
SE_10873 | chr8:11346156-11419244 | CD20 | SE_58515 | chr8:11271776-11367112 | Ly1 | SE_58915 | chr8:11337047-11366620 | Ly3 | SE_60852 | chr8:11348635-11365579 | DHL6 | SE_60985 | chr8:11340629-11417326 | HBL1 | SE_61957 | chr8:11337538-11367440 | Toledo | SE_62362 | chr8:11308990-11367697 | Tonsil |
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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 | GCAGTGAAAG GGGCCATCTT CCACCCTCCC CTGCTGGTCA AGTGCATCTT TCCAGGTTCC 60 GGCACTCCAC GTTGCCACCC AGACAAGTGT CCTGTGGGAA CTAGCAAGTG GGAATCAAAA 120 CTACCCCCAG AGAGGCTCCT GGCCGGGAGA TGAAGGGATC TACCCTGGGG CTAAAGTCTC 180 CCCAGCCTTT CTTGGAGCTT AGGTCCTGGC TTTAGAAAGA TCCCATTCAC ATCCAGGCAC 240 AGTGGCACAC ACCTGTAATC TCAGTACTTT GGGAGGCCGA GGCAGGCGGA TCACTTGAGG 300 TCAGGAGTTT GAGACTGGTC TGGCCAACAT GGCGAAACTG TCTCTACTCA AAATGCAAAA 360 ATTAGCTGGG TGTGGTGGTG TGCGACTGTA ATCCCAGCTA CTCAGGAGGC TGAGGTAGGA 420 GAATTGCTTG AACCCAAGGA GGCAAAGGTT GCAGTGAGCT GAGATCGCAC CATTGCACTC 480 CAGCTTGAGC AACAGAGCGA GATTCCATCT CAAAATAAAG AAAGGAAGGG AGGAAGGAAG 540 GAAGGAAGGA AGGAAGAAAG AAAAGAAAAG AAAAGAAAAG AAAAGAAAAG AAAAGAAAAG 600 AAAAAAAAAA GAAAAGATCC CATTCACCTG CACAAAAGCC ACACCCCTTT GTGGCCAAGG 660 AAAGGGCCAC AGAAGAAGAA GTAGGCCCTT CAGAAGGGGG AGAAGTAGGC GCCTTCAGAA 720 GCTGGTTATC CGTGTGTAAT GCCATCACAG GGACGTGCGT TTAAGATCTT TTATCAGTCT 780 TCGTAGCTAA ATACTTTTAG TTAATTGCAG GCGGGAGGGG CTACTAGCTC AGGCTACATG 840 GAGCATGTGC TCAAAAACTG TCTCCAATAT GGTGACTTGC TGTTTGAGGA CGGTCTAAGC 900 GACTGAGGAG TGTGCCCCCT GTTCCCACCC TTGAGATGAG GCCTGATAAG GGTGCTGGCA 960 TATTTAGTGT TGGGCACCCT GGTGCTCTCC AGCATGTGGT GTTTGGCCTA AGTGGCCCAT 1020 GTGGACTTTG TTTCAAGGAT TTTACGACAA GAAACACCAA AATGAGGACA TCTCTGTGGC 1080 CATGTTTCAG GCAAGGGGGT AATGGATACA GAGCATATGT ACACACAAAC ACACATGCAC 1140 AGAGACACGT ACAGACACAT ACATGCACAC AGACACATAG ATACAGACAC ATACACATAA 1200 GAATACACAC AGAAACACAC AGACACCCAC ACATATACAC ACATGCACAG ACATGTAGAA 1260 ATACCTAGAC ACAGAGGAAC ACACAAAGAT ACACAGGCAC ACATACAGGT 1310
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