Tag | Content |
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EnhancerAtlas ID | HS129-17638 |
Organism | Homo sapiens |
Tissue/cell | MCF10A |
Coordinate | chr19:7547100-7547920 |
Target genes | Number: 22 | Name | Ensembl ID |
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TF binding sites/motifs | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
EBF1 | MA0154.3 | chr19:7547454-7547468 | ATTCCCAGGGGATT | + | 6.12 | EBF1 | MA0154.3 | chr19:7547454-7547468 | ATTCCCAGGGGATT | - | 6.46 |
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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 |
GH19I007482 | chr19 | 7547253 | 7549438 |
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Enhancer Sequence | CAGGACCAGG AGCAGAGGGG GCCTAGGGTC AGACTTACCC ACTGCCCATT TTAGCACCGT 60 AGCCATGCCA GGTGGCAGAG AGCTATTTCC TGACCCCAGT CCCTGGGCCG TGTCCAGGCC 120 TGGCAGGCCC CGCGGGAGAA AGGCTCTGGG GCTGGGGTCC CCGCACAGGC CTGATTTCTG 180 TGTCTCGGCA GCACGGTGCT CAGTGCCCCT TGGAGGGAGG CTCTCAACGC AGCTGTGCAG 240 TGCAGTCCTC TGCAGAGCTT CAAAAACCCC ATGCCCAATG CCAGCCGTGA GGATTCTGCC 300 TCACTCAGCC TGGGGCAGGC CCCAGTACCG GGAATTTTCA CAGGGAATTT TCACATTCCC 360 AGGGGATTCC CAGGCCAAGT TGGGAGCCCT GTGTCAGAGC CTTCCTTCCC AAAGGCTTCC 420 AGTTCCTGCA CAGGTGGGGA CCTCTGTTGC CAGACTCTAT GCAGGGAGCA TGAGGTGGCC 480 CGCAGCGAAC CCTGACCAGG CTGAGATGGT GTGCCAACCC TTGGGCCACC GCACGCCCAC 540 TGCTGACCAC GCGCCAGGCA CAGTGCGGCA AGGCTCATGG CCTCCCTCAA CTCCGAGCAA 600 GTTACAGACG GCCACGCTGA GGCTCTCAGG GAAAGCCGCT GGCCCCCAGT TCCGGCAGGG 660 ATGGGCCTCC AGGCCCTCGA ATTGCAATGC ACACGCGGGC TCTCGGTCCT GCACAGTGCC 720 CATACCCTCT GCCCCAAGTT CTTAATCACA CGGCCTAGAG CCAGCGAGGC AGGACCAGTT 780 GAGGCTGTAG AAACCAGCGC TGAAGCCTGG TTTCTGGGAC 820
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