Tag | Content |
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EnhancerAtlas ID | HS109-03020 |
Organism | Homo sapiens |
Tissue/cell | Kasumi-1 |
Coordinate | chr10:70988450-70989680 |
TF binding sites/motifs | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
EWSR1-FLI1 | MA0149.1 | chr10:70988669-70988687 | AGAAGAAAGAAAGGAAAG | + | 6.04 | EWSR1-FLI1 | MA0149.1 | chr10:70988625-70988643 | GAAAGAAAGAAAGGAAGA | + | 6.22 | EWSR1-FLI1 | MA0149.1 | chr10:70988673-70988691 | GAAAGAAAGGAAAGAAAG | + | 6.33 | IRF1 | MA0050.2 | chr10:70988688-70988709 | AAGAAGAAAGAGAAAGAAAGA | - | 6.72 | IRF1 | MA0050.2 | chr10:70988702-70988723 | AGAAAGAAAGAGAAAGAAGAA | - | 6.77 |
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| Number of super-enhancer constituents: 3 | ID | Coordinate | Tissue/cell |
SE_27984 | chr10:70979065-70991295 | Fetal_Intestine | SE_28850 | chr10:70988580-70990910 | Fetal_Intestine_Large | SE_53047 | chr10:70986422-70990508 | Small_Intestine |
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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 |
GH10I069227 | chr10 | 70987399 | 70991090 |
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Enhancer Sequence | ACCTCTACTA AAAATACAAC AATTAGCCAG GTGTGATGGC ATGCACCTGT AATCCCAGCT 60 ACTCGGGAGG CTGAGGCAGG AGAATCACTT GAACCTGCAA GGCAGAGGTT GCAGTGAGCC 120 GAGATTGCGC CACTGCACTC CAGCCTGGGT GACAGAGCGA GACGCCATCA AAAAAGAAAG 180 AAAGAAAGGA AGAAGAAAGA AAGAAAGAAA GAGAGAGAAA GAAGAAAGAA AGGAAAGAAA 240 GAAGAAAGAG AAAGAAAGAA AGAGAAAGAA GAAAGAAAGA AAGCAAAGAA AAAGAAAGAA 300 AGAAAGAGAG AAAGCTGCCA TTTACTGAGC AACCACTGTG GTCATGGGGT GCTGGGGACT 360 CGCTGAGCCA CATATTTCCT GTGACAACCC TGTGGTGTGG CTGTTCAGAC AGAACCACCA 420 AGGACCAAGG GGTTTCTCCC ATGTCAGGGT CCCAGTGCCC AAACCGAGCT CGTGAAAGAG 480 CACTGGGGCT CTCGCAGGAG CAGGGTCTGA GGTTTGGGAG CTCTCAGGGG GCTTTGATGG 540 GATCAGTCGT GTTCTGGACC TCTCTGGAGC AATGCCTGGA TCAAGGTAGC TTGGCTCTGC 600 TGGTTGAGAG GCCCTGGGAC ACTGCACTGG GAAAGGCCCT GTGCCCTCAC TTGTGGGTAG 660 GTGCTTGGGA TGGACAGTGC CCTGTCCTGG AAGGACGTTG AGCTTCGGAG AGAGACAGCC 720 CTACTTTGAA ATCTTGGCTC TGTCCTTGCC ACAGCTTGAC GAGAGTACTG GGACGTGTCC 780 TTGACAGGGC ATCTGGGGCC CCTGGGAGGA AGCAGCTGAG TCATGTGGGG AGCACCAGGG 840 CTAAGTCCGC CTGGCTTCCT GGACTGCAGC CCCTCCTCCT GATACAGACA AGGTGTGTCC 900 CCAGAAGCAA GGGAAGGTGG CCTTTGATGG TCTGGAGGCT CTGGGACAGG CGGTGTCCTC 960 CTGGCCCTGG CTGCTTCTGA AGGTTCAGAA GTGAAACTAA CTAAGTCATA GAAACTCTCT 1020 CCTCCTTAGC CGGGAAGACG CCCAGCTCCC CATCCCCGTC TCCGCAGAGC CTCTCACCAC 1080 ACAAAGCATC TCACCAGTGA TTCTGTTGTG CCGAGGTCCC TGGGCCCAGA GTCCCTAATA 1140 AGCCAGGTGT TCTTGGTAAA TCCCGGCACC ATACATGATT GTCAGGATTT AATGAGATCA 1200 TGTGGATGGC GTGCTTTAAC ATCTCTAAAA 1230
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