| Tag | Content |
|---|
EnhancerAtlas ID | HS151-01825 |
Organism | Homo sapiens |
Tissue/cell | OCI-LY1 |
Coordinate | chr11:17421400-17423170 |
TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| EWSR1-FLI1 | MA0149.1 | chr11:17421560-17421578 | GGAAGGAACGAAAGAAAA | + | 6.18 | | SPI1 | MA0080.4 | chr11:17422105-17422119 | AAAATGGGGAAGTG | + | 6.33 | | SPIB | MA0081.2 | chr11:17422107-17422119 | AATGGGGAAGTG | + | 6.18 |
|
| | Number of super-enhancer constituents: 3 | ID | Coordinate | Tissue/cell |
| SE_51469 | chr11:17421985-17424486 | Skeletal_Muscle | | SE_65430 | chr11:17421352-17422400 | Pancreatic_islets | | SE_65430 | chr11:17422486-17423552 | Pancreatic_islets |
|
| | Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder | | Number of disease enhancers: 2 | Chromosome | Start | End |
| chr11 | 17421716 | 17422200 | | chr11 | 17422924 | 17422978 |
|
| | Number: 2 | ID | Chromosome | Start | End |
| GH11I017399 | chr11 | 17421353 | 17422400 | | GH11I017401 | chr11 | 17422656 | 17423056 |
|
Enhancer Sequence | AGGTCCTCAT CATGTTTTCC CTGAGTTACT GCGCATGGAC CTGCCTCCTT TCTCTGATCA 60
ACCTGGGCTG CCGTCATCAC TCTCCTTGGC CGCTTCCCTC AGACCTTGCT GACGTAGGCC 120
CGGCCCAGAG GAGATGCAGG AGCACTTGTT TGATGATGGA GGAAGGAACG AAAGAAAAGC 180
TGCCTCATCA TCGCTGGTTT GATAGGACCA AACTCAGGGG ACACGGAGGC ACCCAAGACG 240
TACCTTACTG GGCATTTGCT TTTCACCCTG GAAGGTGTTA GTTCAGCTTT GATTGTCTCT 300
GCGTGGAGAG AGGGCATGTG TCTGAGGGGA CTGAAGGGAG GTTCTGAGGT GGGAGAGAGC 360
ATGCTACTGC ACACCCCCAG GGTGGAGACG TGTGGGAGGG TGACGTGTCT GCAGTGAGTG 420
TGAAACCATG CCTGAAGGGT AGAGTAAGTG CGTGTTGAAA ATGTGTGTGC ATCAGGGCAT 480
GTGCGTGTTA TAGGAGTGTG AGGCGCTCAG CGTATGTGGG TCTCAGGACT GTGTGAGTTG 540
AGGGTCGGCA AGTGTGAGAT GGGAGCTTCT GCCACAGGCG TGCGACAGTG TGTCTGAGGA 600
CTAGAAAAGA GCCCCAGCCT CGGAGCCATG TAAACCCAGG TTGGAGCCTG AACATCACAA 660
CTTCCTGGCT GTGTATCAGG ACTGAGACTC AGTTTTCTTA TGAAAAAAAT GGGGAAGTGA 720
TAGTTCCTAC ATGAACGAAA ACAACCTCCG AGCCCGCCAC TGAGCCCAGT GCTGGGCACT 780
CTTGAAACTC TTTTGGGAAA AAATAAGATC TCTTAGGAAA GCCCAGAAGG TCAGGCAAAC 840
CTGGGTTCCA AGCTCAGCGC CAGCCCCCGC AGTCTGTGTG ACCTTGGATT GATTACCCAG 900
CCTCTCTGGG TCTCGCTTCT GCATCTGGAG AATGTGGCGA TTCGTACCTA TGTTATGTGG 960
TCCTTGTGAG GATTAAATGT AATAATGCAC ATACAACACT TAGCACGGTG CCTGGCATAC 1020
AGTAAGTGGG CAATCAATAA GTGCTAATAG CTCTCAACAG GCTGCTGGAT TAAAGCCAAT 1080
GCATTAAATG TGTATGGGGT TGATTAAAAA GCCTTTCATT CAAATTTAAA AATCATTCAC 1140
CGTGTCAGTA GGGTGTGGAA GACCTCACTG GGTAGCAGTG GCTCTGGCTG ACCACAGGTT 1200
TGGCCTGATC TGAGGCTGTT TACAGGAAGC TGGGATCTGC ACACAAGGGG CTGTGGCCCA 1260
CTCTAGAAGA GTCACCATCT CTCTACCCCA GGGCCCTCTG AGACACCAAT TGAGAGAGGG 1320
AAATCACCAA AACTTAGAGC AAAGGCTAGG CTCAGTAATG TCGAGGGACC TGGAAGTTGA 1380
AGGAACGGGA GAAGTTCAGG CTTGAGAAGA GGAGGCTGGG AGGAGACTCT AGAGTCATAA 1440
TCCAGTCCCC AGCAAGCTTC TTTGTGGAAG ACACAGCATA GGCTTGTCCA GGGGCAAGGG 1500
ATGTCCAGGG AGCAGCGCCA AGGCCAGGGC AGAGCTTTGC TCTGCTCTTC TTTACTTAGA 1560
CAAGATCCCT AAGAGGTGGA TTTCCACTGG CCCTAGGTGC TCCAGGGTGG GCAGAGGGGC 1620
CTGGATACCT CTCCAGGGCT GAAGCTGGAC TTCAGGGGTT GGGGGGAGGA GATGTAAGCC 1680
TCTCTGGCCC TTGGCTGGTC CTTGTGCCCT ATGGTTACTC CTGGACACAG TGCTTGGTGT 1740
CTCATGGTTA CTGTCATACT TCGTGCAGCT 1770
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