| Tag | Content |
|---|
EnhancerAtlas ID | HS105-25605 |
Organism | Homo sapiens |
Tissue/cell | IMR90 |
Coordinate | chr14:93192070-93193290 |
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 |
|
| | 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 |
|
Enhancer Sequence | CCACCATGCC CGGCTAATTT TTGTATTTTA GTAGAGATGG GGTTTCACCA TGTTGGCCAG 60
GCTGGTCTCA AACTCCTGAC CTCAGGTGAT CCACCTACCT TGGTCTCCCA AAGTGATGAA 120
ATTACAGGTG TGAGCCACCA CACCTGGCCA CGGATTTTTT TAAATATAAA AGTGATATTG 180
TGCAACAACA TGGATTAATC TCAAAACACC ATAAGTTATG AGCTCATCTG ACCGGGCACA 240
GTGGCTCATA CCTGTAATCC CAGCACTTTG GGAGGCTGAG GCAGGTGGAT CATCAGAGGT 300
CAGGAGATCG AGACCAGTCT GGCTAACATG GTAAAACCCT GTCTCTACTA AAAATACAAA 360
AATTAGCCGG GCGTGGTGGC AGGTGCCTGT AATCCCAGCT ATTCGGGAGG CTGAGACAGG 420
AGAATCGCTT AAACCCAGGA GGCGGAGACT GCAGTGAGCT GAGATCACGC CATTGCACTC 480
CAGGCTGGGC AACAAGATTG AGGCTCTGTC TCAAAAAAAA AAAAAAAATT AAATAAGTAA 540
ACAAATAGCT TGTGAGAAAC AGACTGTGAG TCACCACCAC CTCCTTCCTG CACTCCCTGG 600
CCACTCCCTC TCGCCTCCGT CACTGCAGTC TGCCCAGCCT GTCTTTGGCC CCGCCAGCCT 660
CGATTTTTGC CCCTTGGCCC ACAAAACCTC AAATATCTAC TATCTGGCCC TTTATAGAAA 720
AAAACTCTGC AGGCCCCAGT CTTGAGCCAG ACAGCAATGG TGAGGCTCTG AGTGTGTGGG 780
GGTGGGGAAG GGGCTTGCCA GGAGCACACA GAGTGAGGAG CTCCCTGTTC TTGTCATTGG 840
TGACATGGCG CCTGTCCAAC CCTTTATCTA CTTCTGAGTG GAGAGGTTCT GTCAAAGGGA 900
AAGAAAGGGA GAGTTGCTGA CTGGGCCTTC TCCTCCTAAC ACGCCTCACC ATGCCCTCAC 960
CCTACCTTGC CGGTCTCCTT CTCCCTCGCT TCCTCCTCCC CATCTACCTG GGCCATGCAC 1020
TGTCCTTGCA TGCCCTGTGG CCACCTTCCT TTCCACCAGG GCCCTGGCTT TGCTCAGATG 1080
ACCTACCCAG CTCCAAGTGG TCACAAGTGG TCAGGAGCTT CCCTGAGTGT GAACTGGAAA 1140
TCCATTTCCC CTCACCAGGA ACTGACTGAC TTGAACATGA GCACGTGATG CAATTCTGGC 1200
CAGGAAGACT CGGGACAAAG 1220
|
