Tag | Content |
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EnhancerAtlas ID | HS092-16822 |
Organism | Homo sapiens |
Tissue/cell | HFF |
Coordinate | chr14:93192450-93193260 |
Target genes | |
TF binding sites/motifs | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
FOXP2 | MA0593.1 | chr14:93192604-93192615 | AAGTAAACAAA | + | 6.62 | ZNF263 | MA0528.1 | chr14:93193051-93193072 | TCCCTCGCTTCCTCCTCCCCA | - | 6.06 | ZNF263 | MA0528.1 | chr14:93193045-93193066 | TCCTTCTCCCTCGCTTCCTCC | - | 6.76 | ZNF263 | MA0528.1 | chr14:93193048-93193069 | TTCTCCCTCGCTTCCTCCTCC | - | 7.65 |
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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 |
GH14I092723 | chr14 | 93189754 | 93193617 |
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Enhancer Sequence | AGGTGCCTGT AATCCCAGCT ATTCGGGAGG CTGAGACAGG AGAATCGCTT AAACCCAGGA 60 GGCGGAGACT GCAGTGAGCT GAGATCACGC CATTGCACTC CAGGCTGGGC AACAAGATTG 120 AGGCTCTGTC TCAAAAAAAA AAAAAAAATT AAATAAGTAA ACAAATAGCT TGTGAGAAAC 180 AGACTGTGAG TCACCACCAC CTCCTTCCTG CACTCCCTGG CCACTCCCTC TCGCCTCCGT 240 CACTGCAGTC TGCCCAGCCT GTCTTTGGCC CCGCCAGCCT CGATTTTTGC CCCTTGGCCC 300 ACAAAACCTC AAATATCTAC TATCTGGCCC TTTATAGAAA AAAACTCTGC AGGCCCCAGT 360 CTTGAGCCAG ACAGCAATGG TGAGGCTCTG AGTGTGTGGG GGTGGGGAAG GGGCTTGCCA 420 GGAGCACACA GAGTGAGGAG CTCCCTGTTC TTGTCATTGG TGACATGGCG CCTGTCCAAC 480 CCTTTATCTA CTTCTGAGTG GAGAGGTTCT GTCAAAGGGA AAGAAAGGGA GAGTTGCTGA 540 CTGGGCCTTC TCCTCCTAAC ACGCCTCACC ATGCCCTCAC CCTACCTTGC CGGTCTCCTT 600 CTCCCTCGCT TCCTCCTCCC CATCTACCTG GGCCATGCAC TGTCCTTGCA TGCCCTGTGG 660 CCACCTTCCT TTCCACCAGG GCCCTGGCTT TGCTCAGATG ACCTACCCAG CTCCAAGTGG 720 TCACAAGTGG TCAGGAGCTT CCCTGAGTGT GAACTGGAAA TCCATTTCCC CTCACCAGGA 780 ACTGACTGAC TTGAACATGA GCACGTGATG 810
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