| Tag | Content |
|---|
EnhancerAtlas ID | HS108-26438 |
Organism | Homo sapiens |
Tissue/cell | K562 |
Coordinate | chr22:20772160-20774210 |
TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| CTCF | MA0139.1 | chr22:20772592-20772611 | CAGCCGCCAGATGGCAGCA | + | 6.24 | | EWSR1-FLI1 | MA0149.1 | chr22:20773760-20773778 | CCTTCCTCCCACCCTTCC | - | 7.07 | | NR2C2 | MA0504.1 | chr22:20773865-20773880 | TGACCTCTGCCCTCC | - | 7.11 | | Nr2f6(var.2) | MA0728.1 | chr22:20773109-20773124 | TGAACTCCTGACCTC | - | 6.22 | | ZNF263 | MA0528.1 | chr22:20773772-20773793 | CCTTCCCACTCCTCTTCCTCC | - | 6.95 |
|
| | Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder | | Number of disease enhancers: 5 | Chromosome | Start | End |
| chr22 | 20773284 | 20773400 | | chr22 | 20773400 | 20773803 | | chr22 | 20772547 | 20772776 | | chr22 | 20773296 | 20773738 | | chr22 | 20774009 | 20774124 |
|
| | Number: 1 | ID | Chromosome | Start | End |
| GH22I020417 | chr22 | 20772081 | 20773129 |
|
Enhancer Sequence | TGAGGTCAGG AGATCGAGAC CAGCCTGGCC AACATGGTGA AACCCCGTCT CTACTAAAAA 60
TACAAAAATT AGTCGGGCTT GGTGGTACGC GCTTGTAATC CCAGCTACTC TGTAGGCTAA 120
GGCAGGAGAA TCGCTTGAAC CTGGGAGGCA GAGGTTGCAG TGAGCCAAGA TTGCGCCACT 180
GCACTCCAGC CTGGGCGATA AAGTGGATAC TCTGTTTCAA AAGAAAAAAA AAAGGTGGCA 240
CCGGCCCGGT GCGGTGGCTC ACACCTGTAA TCTCAGCACT TTCGGAGGCT GAGATGGAAG 300
GATGTCTTGG GCCCGGGGGA TGGAGGCTGC AGTGAGCGGT TATTGAGTGA CTGCGTCCAG 360
CCTGGGCCTC AGAGTGAGGC CGTGCCTCAA AAAGAAGAAA AAAAAAAAAA AAAAAAGCAG 420
CAGCTACCCA TCCAGCCGCC AGATGGCAGC ACGATTCCAT GGCCCCCACT AGCCGCTGGC 480
TGCCTGGTGC CGGATGCAGT CCGAAAGGCG GTTCTGAGCT CCAAGGGCCG GCGCCGCGCG 540
TGCCTGCGGT CCCAGCTGCT CGGGAGGCCC AGGCAGGAGA ATCGCGTGAC CGGGAGTTCT 600
GCGCTGCAGT GCGCTGTGCC GATCCAGGTC CTCACTGAAG CCGGCATCAG TATGGTGGCC 660
TCTGCCACCA GGCCGCCTAG GGAGGGGCGA GGCAGCCCCA GTTGGAAACG GAGCGCGTCA 720
GTAGTGGCAT CGCGCCTGGG AATAGCCTCT GCGCTCCAGC CGGGTCGACC TGCCGAGACT 780
CCGCCTCTAA AACCAGCAAA TACCGGGAGG CTGAGGGACG AGGACCGCTG GAGCCCGGGA 840
GGCGGAGGTT GCAGTGAGTA GCTGGGATTA CAGGCAGGCG CCACCACGCC CGGGTAATTT 900
TTGTGTTATT AGTAGAGACG GGGTTCCACC ATGTTGACCA GGCAGGTCTT GAACTCCTGA 960
CCTCAAGTGA TCCACCCTCC TTGGCCTCCC AAAGTGCTGG GATTACAGGC GTGAGCCATT 1020
GCGCCTGGCC AAATAAGTAA TTTAAGCAAT TTTTTTTGTT TCAGAAAAAA AATTAACTCA 1080
TAAAGGAGCC CCCCCGACAC ACACACACAC ACACACACAC ACACACACAC ACACACACAC 1140
ACGGGAAGCA GCAGTGTAAT TGGAATGCCC ACTGCTGAGG CTCTCGAATG AGTGTCATGT 1200
GTGCACATTT TGCCCCTCAC AATGCACGTC AGACTATTAA TAGGAAGCAG CCGCTGGAAT 1260
ACCTCTGGTG GGGTGTGTGC AGCAGGCAGC TTTGGAATTA CGGTATCCCC AATGTGACAG 1320
CAGGACAATG GCTTCTTCAC TGGCACTGTC CAACCACAGT GCTGTGGTTA TGTCTCGAGG 1380
TCCATTATTG GGCGAAGGTC ACTGCAGACT CAGGGAGGCC CAGGAGCTCA CCCCAACCAG 1440
CTTCTTTACC AGGTGAGTGA CCTCAGCCCT GCAGCTGGAC TCATGGAGAC AATGACCTCA 1500
CCCGAAGATA GATGACCCCT GTCCACCGTC CACACAACAA CTGAACTGGC CCCAGGTTGA 1560
CTCCTCTACA CCCTGCTTCC TACTGTACCC CTGTCAAAGG CCTTCCTCCC ACCCTTCCCA 1620
CTCCTCTTCC TCCCTGGCAG CCCAACCACC ACAAATTCAC TAACTTGTTT TCAACTCTTA 1680
CAGGCTGCCC TCCTAACCCT AGCCCTGACC TCTGCCCTCC TAACCCCAGC CCTGACCCCA 1740
CCGCCCTCTC AGGAGGCTTT ACCAATCCTC TGCATGTTAG CCCCACCCAA GGAACAGGCC 1800
TATTTTCAAG CATACTAACT GTTGGGTGTG TCGCTTACCT ATGCATATGA CAGCCAATCC 1860
AACCTACCTA AATGACAGCA CAGCTCCATC CATGGATGTG GCTGATCACA TCTCCAAACC 1920
ATCTTCCCAC TGGGGACAAA TTCTTGGATT TTTTAGAGAC AGGTTCTCAC TCTGTCACCC 1980
AGGCTGGAGT ACAGTGGTGA GCCTCAGACT CCTGGGCTCA AGGGATCCTC CCACCTCAAC 2040
CTCTGGAGTA 2050
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