Tag | Content |
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EnhancerAtlas ID | HS092-38936 |
Organism | Homo sapiens |
Tissue/cell | HFF |
Coordinate | chr9:132004820-132005900 |
Target genes | Number: 26 | Name | Ensembl ID |
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TF binding sites/motifs | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
REST | MA0138.2 | chr9:132005828-132005849 | ATCAGTGCCTGGGACAGTGCC | + | 6.08 |
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| Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder | Number of disease enhancers: 2 | Chromosome | Start | End |
chr9 | 132005480 | 132005830 | chr9 | 132005135 | 132005862 |
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| Number: 1 | ID | Chromosome | Start | End |
GH09I129242 | chr9 | 132004868 | 132005869 |
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Enhancer Sequence | TTTTAGAGGA TCTCTGAGGC TACTGGGAGG AGAAGGCGTG GAGCTGGGTG AGAATGGAGG 60 CAGGGAGGCC TAGGAGGGGC TGGCGGTGAT GAGGCTGGGG TTGAGGAGGA GGCCGCAGGA 120 AGGGAGACAA AGGGAGGCAT TTGGAAAGCA TCCAGAAGTC GCGTGGCTGG GACCTGATAA 180 CAGGTGTGAG CCAGGGGCTG AGAGGCAGGG AGGACTTAAG GTATGCAAGG ACAGCTGAGG 240 GAGGATGGGT GTCATTCGCA GATTGGAGGA GCCCTGGAGG AGGAGCCAGT CTGGCTGGGG 300 TGCAGGAGGG CAGGGTGACA AAGATCCAGT TTTGGCCAAG GTGCCTTTGG GTCATGAGTG 360 GGGACATGCA GTGTCTGTGA GGGTGGCTGG GATTTCGGGG CAGCCATGAT CCAGTCGAAG 420 CCCTTCCCCA GCCCCTGGCC TCCAGCAAAA TCAGGACTTG GGGCCTGTTC CTTGGGGCCT 480 CGGGAACACG CAGATCTCAT TCCCCGCCCC AGTTTCTCTG GAAGGAAAAC ACCCAGGGCC 540 TCGGTGGAAC CGGCATTAAT TTCCCCTGTT CGGCTCATCA TTCCATCATC ACGAGAGAGC 600 CAAACAGATG ACCATTTCGT CATTGCATAT GCCCATGCGG GGCTTCCGTA ATCTGATCAC 660 TTAATCACAT GCTTATTCCA TGAGGACGGA GGCACGGGCA AGCTCTGGGG CCCACTCCTT 720 GGGCAGCGCA TTTTGGACCA AGTCCCTTAG CGTTCCTGGC TGCCTCTGTT TCTCTGCCTG 780 CCTTGGGAAT CCAGACAGCC TCATGACAAG AGGAGATGAG GCAGTGGTTG CGGAAGAGCC 840 TGGTCTCTCA GCCACAGCAG CCACGAGGTG CTGGCAAGCT CTCTGCAGCC TGTGCTGCTG 900 GGAGGTAGAG GCTTCGGCAG CTTGTCCTCC TTGTGGCCTA ACACACGCTG CCCGTCTCCC 960 CACTTGCATG GAAGCCCCAG GAGGACACGC AGTTTGTCTC TTTGGTTCAT CAGTGCCTGG 1020 GACAGTGCCT GGCACATGAG GGAGCTTAGG TGAAGTTTAT CGAAATTTCC CATTTGTCTT 1080
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