Tag | Content |
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EnhancerAtlas ID | HS129-17702 |
Organism | Homo sapiens |
Tissue/cell | MCF10A |
Coordinate | chr19:8605480-8606070 |
Target genes | Number: 15 | 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 |
|
| Number: 1 | ID | Chromosome | Start | End |
GH19I008540 | chr19 | 8605581 | 8606246 |
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Enhancer Sequence | CTACTCGGGA GGCTGAGGCA GGAGAATCGC TTGAACCCAG GAGGTGGAGG TTGCAGTGAG 60 CCGAGATCGT GCCACTGCAC TCCAGCCTGG GCGGCAGGGT GAGAGACACT GTCTCCAAAA 120 AAAAAAAAAA AAAATCGGAT TGTGGTGATG GTTGCGCAAT TCTGTGAATT TGCTAAACGT 180 CATGGATTGA GACACTGCTT AAAGTGGGTG GATTTAATGG TAAGTGCTGC TGAAACCCTT 240 ACGTGCACAT GGATCCCTGG GAGGCATGGG TGCATCCTGG CTTAAAGATC AGGTTAGGTT 300 CCGATAGTTC TAAACCTGAT TGTTCAGATT CTGATAGTTC AGAATCAGAT GCAGATTCTG 360 ATTCTGGAGG TCTGGGGTGG AGTTTGAGGT TCTGCCTTTT TTTTCCCCTC AGAGATAAGG 420 TCTGTTGCCA AGGCTGGAGT GCAGTGGTGC AATCACGGCT CACTGTAGCC TCCACCTCCT 480 AGGCTCAAGT GATCCTTCTA TCTCAGCCTC CCGAGTAGCT GGGACTATAG GCATGTGCCA 540 CCACACCCAG CTAATTAATT AATTATTATT ATTTTTGCTG GCAGAGTAGA 590
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