Tag | Content |
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EnhancerAtlas ID | HS080-02631 |
Organism | Homo sapiens |
Tissue/cell | H9 |
Coordinate | chr1:182668270-182669800 |
TF binding sites/motifs | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
HEY2 | MA0649.1 | chr1:182668684-182668694 | GACACGTGCC | + | 6.02 | Npas2 | MA0626.1 | chr1:182668684-182668694 | GACACGTGCC | - | 6.02 |
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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 |
GH01I182698 | chr1 | 182668125 | 182669832 |
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Enhancer Sequence | CGCCTCTCCA GCTGCTGTAC TTTCATCACC CTGCATGCCT CCATCCCTGG GCCAGAGGGG 60 TTTCCACATC ACCACAGAGG CAGGCCTTCC TTCATTTTAT TTATTCCATT TGGGATTAAA 120 CACATTGAAA GGGGGCCATG GCTAAATGGG TGTTTCTCGC CTGGCTCGGT ACTTAGAAAT 180 CAAAGAAGGA GCTTCATGGT GTATGTGGAA GGGGATGGAG TGTAGAGAGG AGGAGGTGGT 240 TTCTGCAGAC AGGCAGCTCT TCCCATCTTC CCAGGAGCAA AGATTAGTTC CCTGGGCCCA 300 GGCCTCAGTG GCAGGGGGCC AAGGAAAGCA GGCCCAAGGC CTTTCCTAAC TCTTAGCCCC 360 CAGGGATTGG CACATGCCAC GGGGAAAGTG AAAAACATTT TACAAAACAG GCTAGACACG 420 TGCCACATAG CTGTGTCCTT AGAAACTTCC ACACAGATCC CTGTTGGAGG CTCTTCTCCC 480 TGTGCTGTGG CTCCCCAAAG CCTGCTTCGT TGCTGCAGGG ACCTTAAGAA TCCGAGGGGA 540 TTCACAGAGC CCTGGGGATT GCAACGGGAT TACCGGGGAG GGATACAGGC AAAATCCCCT 600 GAGAGGCCTG CAATGTGCTG CAGGCCTGGG GCCTTCCTGG CAGGATGGAT ATCTCTATTC 660 CTGGAGCCAA AAGTTCTGGG ATCTGCAGAA AGGGATCCCT CGGGGACTAT AATGAATGCC 720 GTGTTCCAGC AGTGCCAGCT CGGTTCAGCT GCTTGATTAA TGACATATGA GAGGTCTCAC 780 GGCAAATTTA ACAGGAGGGC GCACCCTCAC ACAGTGCCTG CCCTGGATAA GATCCGGCAC 840 CTCACACCCT GCAGGAGACT GGAGGGGCTC ACAGAACTCC TTCCCGAGCT CGGGATCCAG 900 GGCGAAGCCT GTGAAGAGCC CGCCTGGGTC TCAGGTTCTG AGTCTTGAGT GCATAACAAT 960 GCGCCCCAGA GCCCGCCGAG GGGAGAACTA GCTCCATCTG CTCCTTCCCA ATTCTCGGCT 1020 CCGGCGAGGG GGAGGGGGAT CCCTCGGCGG TTAGGCCGGG TCCTGCACGG TTATTGGCTG 1080 ACACATTTTC AAAGCTACTC TCAAAGGCTT TTATGAAAAT GCTGTTGCCG GGCAGCAGCT 1140 GAAGCCATTT GCCCTAGAAA ATGGATGGAA GCAGGTGTAA CCACTCACCC CAACATGACC 1200 CCCAAAACAT TCCCCGCGAC ACACACGCTA GTCTACAGTG TGTTACTTTG TCCCTGTATA 1260 TTTCAATAAG CGCACCAATC TGACACCTCA GCATTCCTCC CCGAAAACGT AACCATGAGC 1320 ATTGTTCTTC CTGGTTTCTC TTTCAAGAGA AAGGAGGTGC CAGTCCAGGG TGGTATTCCA 1380 AGAGACACCC CAGGTTCAGC CTCGGGCTGC CTCTGGCGGC AGAAGACACA GGGTGCATCT 1440 TCCGTCTTCT AATTCCCATA GCTTTCAGGA GATAGCAGAA TTGCTGGAAG TCATGAGTGT 1500 CTTAGAAAGA CTGAATGCTT TTTGTTAGAG 1530
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