Tag | Content |
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EnhancerAtlas ID | HS105-38778 |
Organism | Homo sapiens |
Tissue/cell | IMR90 |
Coordinate | chr19:8605440-8606060 |
Target genes | Number: 13 | Name | Ensembl ID |
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TF binding sites/motifs | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
Lhx3 | MA0135.1 | chr19:8606028-8606041 | AGCTAATTAATTA | - | 6.09 | Lhx3 | MA0135.1 | chr19:8606035-8606048 | TAATTAATTATTA | + | 6.18 | Lhx3 | MA0135.1 | chr19:8606031-8606044 | TAATTAATTAATT | + | 6.78 | Lhx3 | MA0135.1 | chr19:8606032-8606045 | AATTAATTAATTA | - | 6.78 | POU6F1 | MA0628.1 | chr19:8606033-8606043 | ATTAATTAAT | + | 6.02 | POU6F1 | MA0628.1 | chr19:8606033-8606043 | ATTAATTAAT | - | 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 |
GH19I008540 | chr19 | 8605581 | 8606246 |
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Enhancer Sequence | AAAATTAGCG GGGCATGATG GTGGGCGTCT ATAATCCCAG CTACTCGGGA GGCTGAGGCA 60 GGAGAATCGC TTGAACCCAG GAGGTGGAGG TTGCAGTGAG CCGAGATCGT GCCACTGCAC 120 TCCAGCCTGG GCGGCAGGGT GAGAGACACT GTCTCCAAAA AAAAAAAAAA AAAATCGGAT 180 TGTGGTGATG GTTGCGCAAT TCTGTGAATT TGCTAAACGT CATGGATTGA GACACTGCTT 240 AAAGTGGGTG GATTTAATGG TAAGTGCTGC TGAAACCCTT ACGTGCACAT GGATCCCTGG 300 GAGGCATGGG TGCATCCTGG CTTAAAGATC AGGTTAGGTT CCGATAGTTC TAAACCTGAT 360 TGTTCAGATT CTGATAGTTC AGAATCAGAT GCAGATTCTG ATTCTGGAGG TCTGGGGTGG 420 AGTTTGAGGT TCTGCCTTTT TTTTCCCCTC AGAGATAAGG TCTGTTGCCA AGGCTGGAGT 480 GCAGTGGTGC AATCACGGCT CACTGTAGCC TCCACCTCCT AGGCTCAAGT GATCCTTCTA 540 TCTCAGCCTC CCGAGTAGCT GGGACTATAG GCATGTGCCA CCACACCCAG CTAATTAATT 600 AATTATTATT ATTTTTGCTG 620
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