Tag | Content |
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EnhancerAtlas ID | HS080-21121 |
Organism | Homo sapiens |
Tissue/cell | H9 |
Coordinate | chr20:2686910-2687740 |
Target genes | Number: 12 | Name | Ensembl ID |
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TF binding sites/motifs | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
IRF2 | MA0051.1 | chr20:2687585-2687603 | GGAAACTGAAACCTGAAC | + | 6.18 | RELA | MA0107.1 | chr20:2687502-2687512 | GGGAATTTCC | + | 6.02 | ZNF263 | MA0528.1 | chr20:2687210-2687231 | GGAGCAGGGGAGGGAGGTAAG | + | 6.43 |
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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 | GTGAGTCAGC GCAGAGGGTG CTGAGGCCCA TCTCACTCTC TTCCCGGACC CTGCCTCCCC 60 CTGGTCTGAG TGAGCCTCCT TGTTCCTGCC CTCATCTCCC TATGCCCTCC GTCCCCATCA 120 GCCTAGCTCC CCCAGTTCCC ACCCCAGCCT GTGCCGGAGG GTGTGTGGCT TTTGCCCTCT 180 GTTCTAGAAA AGACAATATT TGTACAAAAA CCCTGGCTTG GGTCATGTTT CCTAGCAGCC 240 CAGCCTTAGA TGGGAACTCA GGTGCAGGTA GTTTATTTGG GGAGATGGGA GGGGCTCCTA 300 GGAGCAGGGG AGGGAGGTAA GCTGGACAGA AAACTGCACA GGGAGCTCTG GAGAAGGAAT 360 GGCACCAGAA GTGTCCCCCC TCGAAGCAAG TACCAGGATT TTGCACCCCG TATCAATTAG 420 TCATTGGCTG GGAACCACTC CTAAGGGTAG CACGTAACCT CTGAGACATT TTCAGACCAG 480 GCAGTTCCTG TCCACTGAGA GCAGTTCTCA GGAGGAAGCC CTCTGCAGCT GACATCAGCC 540 ACAGCCACGG GAAGGTGCAC ATTTCCAGTA AAGGGGATGT GGGCACAGCC CTGGGAATTT 600 CCACTGCAGA CCCTTGCACC TTGCTGATGT GACGGTTACG GGAAGGAGGC TCAGAGGCCA 660 GCACAAGGAG CTGGAGGAAA CTGAAACCTG AACAGGCTCT GATGGATTCT GCCAACACAG 720 GGCCCCAAAT CTCAGGGCTT TTCAGAGAAG CTGTGCATGC TGGCAAGGAG GGGGCTGAGT 780 CTCAAATGGG CCAGATTAGT GGGCTAGGAA TGCAAGCTGG AGATCTGGGC 830
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