Tag | Content |
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EnhancerAtlas ID | HS006-26357 |
Organism | Homo sapiens |
Tissue/cell | Astrocyte |
Coordinate | chr22:42624800-42626180 |
TF binding sites/motifs | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
EWSR1-FLI1 | MA0149.1 | chr22:42625143-42625161 | GGAAGGAGGAAAGGCAGT | + | 6.31 | NFAT5 | MA0606.1 | chr22:42624893-42624903 | AATGGAAAAT | - | 6.02 | NFATC1 | MA0624.1 | chr22:42624893-42624903 | AATGGAAAAT | - | 6.02 | NFATC3 | MA0625.1 | chr22:42624893-42624903 | AATGGAAAAT | - | 6.02 | SCRT1 | MA0743.1 | chr22:42625973-42625988 | AAACACTTGTTGCTC | - | 6.35 | ZNF263 | MA0528.1 | chr22:42625144-42625165 | GAAGGAGGAAAGGCAGTGGGG | + | 6.33 |
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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 |
GH22I042227 | chr22 | 42623540 | 42625810 |
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Enhancer Sequence | ATGAGATCAC CCAGAGCAGT TTTTCAAACT GCAGGCTGTG AAATCAATTT AGTGGGTCAT 60 GAACAGCACT TAAAAAAAAA TGAAATAGAG CAGAATGGAA AATAACAGAG TCCACGGCTC 120 ATGAAGTATA AGAACCGTTT TGTGAAACTT TTGTTTCTGT TGTGTCTGTG TGCACAAGAC 180 GGTGTAGTGT GTTTGTACTT GTCCGGCATT TGGTATGGCT GAACAAAAAG ATTTAAAACC 240 ACTGGTCTAG AGGCTAACTT GGAGTGACTG ATCCCTGCAA TCACTCTATC ATTTAGAAGG 300 TGGAGAAGAG GAAAAGAAGC CAGAAAAGGA GAGTGAAGAA GTAGGAAGGA GGAAAGGCAG 360 TGGGGGGGTC CCAAGCAAAT GTGACATGTT GGACATCCAA CGTGCTGGTG AGAGTCATGC 420 AGTATGATCA CAGCAGAGAT GTCCATAATT ATGGAATGGC AAGGTAAGCA CACAGCTGTG 480 GGAGCAGAGG GGCACCTAAC CTGTTTAAAC TTAGCACAGA ATAAAAAAGG GAAGGAGAGA 540 GGTGATATTA GGATTTTATT TGAGATCTAA GTTTAAGGGA ACGGCAGGAT ATCCAGTCTG 600 TAACTTCCAT AAACAGCAAA TATCCAATCA TTCTTTTATT GTTGTTTTTA AGCATCTACT 660 ATGTGCTGGG CTGTTTACTA GACCTGGGAA AATAACTAGG ACACTGTTCT ATCCTGAAAA 720 GCCTCAAACT GCAAGAGAGT AACGCAGGTA CAGTACAGTG AAGAGAGAGG GTCAGAAGAT 780 AGGGTGCGTA ACAACAGGTT TGTTGAAGGC CACGGCAATT TTCCTTTCCA ACCATACTGC 840 TCACTATTGG CCAAACCCAC CACTCCACAC AGACCATGCG CTCCGACCTC TTGATTTGTG 900 CTTGGCCTCT CCCCAAAACA CTTTCCAAAT CTGAGTCATT CCTCAAGGCC ATTTGGCTTC 960 CTCACTGAAG GCTTCAGGAA AACGGCTCAG CTTGGTGATC TTGCCTTCCC CAAACAGCTA 1020 CAGCACTTCT TGTCCATACA CCATTACCTG GTGGCTGTGT CCTTATTTCC CCACTTGGTA 1080 TGAATGCCTT ATCTCCCCAG CTGAGCCATG TATTGTTGAA GGCATGTAAC AAACATGTCT 1140 CACATCTACA AGGTCCTCAA ACAGCAGCCA AGCAAACACT TGTTGCTCTG CTACTAGACT 1200 TCCCTCCAAT CCAGCTTGCA TTTCAGCATC TTACTGAAAA AGATCTGATT AATTCACCCC 1260 CTATTTTAAA ACCTTCACTG GCTCCCAATT ATTAGTACAG CACATGCAGA CTTGTCTTCC 1320 AGGTGTACCA CACAGCTTTC CCTTCCCTGC CTCCCAAACA CCTTAAAGTT GAAGCAACAG 1380
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