Tag | Content |
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EnhancerAtlas ID | HS184-17716 |
Organism | Homo sapiens |
Tissue/cell | T47D |
Coordinate | chr20:4850150-4850550 |
Target genes | |
TF binding sites/motifs | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
FOXP2 | MA0593.1 | chr20:4850355-4850366 | AAGTAAACAAA | + | 6.62 | FOXP2 | MA0593.1 | chr20:4850390-4850401 | AAGTAAACAAA | + | 6.62 | IRF1 | MA0050.2 | chr20:4850342-4850363 | ACGAGGAAAATGAAAGTAAAC | - | 6.48 | IRF2 | MA0051.1 | chr20:4850346-4850364 | GGAAAATGAAAGTAAACA | + | 6.69 |
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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 |
GH20I004869 | chr20 | 4850221 | 4850450 |
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Enhancer Sequence | GAGCTACTTT GATTTTATCT ATCTAATCTC CAAATGACAC ACACACACAC ACACACCCCA 60 AAAAAAGCAA AGAACAAGTG CAGTGCTTGG CATGTGGTTT TTGAATTTAA GGCTTACAGT 120 GGTTTCGCAG AGAGTGTGTT ATTTGATGTC ACTGCAATTA AGGAAGGGTA GGAATTCCGT 180 TCCACGTCAT GGACGAGGAA AATGAAAGTA AACAAAGGCA GTGGTGTATC AGACAGTCGA 240 AAGTAAACAA AGGTGGTGAT GCATCAAACA GTCGCTAGAG TCCTGCTGCT TGGCTGGGCT 300 CCTGCTGAAA CTCTTGGTTT TGTCTTCAAG GTAATGTAAA CCTAAGAACA AAGTAACAAG 360 GTGCTGGGAC CAATCAGGAA CTTGTCTTCT CAGGAACGTA 400
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