Tag | Content |
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EnhancerAtlas ID | HS094-03002 |
Organism | Homo sapiens |
Tissue/cell | hMADS-3 |
Coordinate | chr1:182668340-182669260 |
Target genes | |
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 | ACCACAGAGG CAGGCCTTCC TTCATTTTAT TTATTCCATT TGGGATTAAA CACATTGAAA 60 GGGGGCCATG GCTAAATGGG TGTTTCTCGC CTGGCTCGGT ACTTAGAAAT CAAAGAAGGA 120 GCTTCATGGT GTATGTGGAA GGGGATGGAG TGTAGAGAGG AGGAGGTGGT TTCTGCAGAC 180 AGGCAGCTCT TCCCATCTTC CCAGGAGCAA AGATTAGTTC CCTGGGCCCA GGCCTCAGTG 240 GCAGGGGGCC AAGGAAAGCA GGCCCAAGGC CTTTCCTAAC TCTTAGCCCC CAGGGATTGG 300 CACATGCCAC GGGGAAAGTG AAAAACATTT TACAAAACAG GCTAGACACG TGCCACATAG 360 CTGTGTCCTT AGAAACTTCC ACACAGATCC CTGTTGGAGG CTCTTCTCCC TGTGCTGTGG 420 CTCCCCAAAG CCTGCTTCGT TGCTGCAGGG ACCTTAAGAA TCCGAGGGGA TTCACAGAGC 480 CCTGGGGATT GCAACGGGAT TACCGGGGAG GGATACAGGC AAAATCCCCT GAGAGGCCTG 540 CAATGTGCTG CAGGCCTGGG GCCTTCCTGG CAGGATGGAT ATCTCTATTC CTGGAGCCAA 600 AAGTTCTGGG ATCTGCAGAA AGGGATCCCT CGGGGACTAT AATGAATGCC GTGTTCCAGC 660 AGTGCCAGCT CGGTTCAGCT GCTTGATTAA TGACATATGA GAGGTCTCAC GGCAAATTTA 720 ACAGGAGGGC GCACCCTCAC ACAGTGCCTG CCCTGGATAA GATCCGGCAC CTCACACCCT 780 GCAGGAGACT GGAGGGGCTC ACAGAACTCC TTCCCGAGCT CGGGATCCAG GGCGAAGCCT 840 GTGAAGAGCC CGCCTGGGTC TCAGGTTCTG AGTCTTGAGT GCATAACAAT GCGCCCCAGA 900 GCCCGCCGAG GGGAGAACTA 920
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