| Tag | Content |
|---|
EnhancerAtlas ID | HS116-11192 |
Organism | Homo sapiens |
Tissue/cell | Left_ventricle |
Coordinate | chr14:93192480-93193420 |
TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| FOXP2 | MA0593.1 | chr14:93192604-93192615 | AAGTAAACAAA | + | 6.62 | | Hnf4a | MA0114.3 | chr14:93193280-93193296 | CGGGACAAAGTCCACC | + | 6.23 | | 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 | CTGAGACAGG AGAATCGCTT AAACCCAGGA GGCGGAGACT GCAGTGAGCT GAGATCACGC 60
CATTGCACTC CAGGCTGGGC AACAAGATTG AGGCTCTGTC TCAAAAAAAA AAAAAAAATT 120
AAATAAGTAA ACAAATAGCT TGTGAGAAAC AGACTGTGAG TCACCACCAC CTCCTTCCTG 180
CACTCCCTGG CCACTCCCTC TCGCCTCCGT CACTGCAGTC TGCCCAGCCT GTCTTTGGCC 240
CCGCCAGCCT CGATTTTTGC CCCTTGGCCC ACAAAACCTC AAATATCTAC TATCTGGCCC 300
TTTATAGAAA AAAACTCTGC AGGCCCCAGT CTTGAGCCAG ACAGCAATGG TGAGGCTCTG 360
AGTGTGTGGG GGTGGGGAAG GGGCTTGCCA GGAGCACACA GAGTGAGGAG CTCCCTGTTC 420
TTGTCATTGG TGACATGGCG CCTGTCCAAC CCTTTATCTA CTTCTGAGTG GAGAGGTTCT 480
GTCAAAGGGA AAGAAAGGGA GAGTTGCTGA CTGGGCCTTC TCCTCCTAAC ACGCCTCACC 540
ATGCCCTCAC CCTACCTTGC CGGTCTCCTT CTCCCTCGCT TCCTCCTCCC CATCTACCTG 600
GGCCATGCAC TGTCCTTGCA TGCCCTGTGG CCACCTTCCT TTCCACCAGG GCCCTGGCTT 660
TGCTCAGATG ACCTACCCAG CTCCAAGTGG TCACAAGTGG TCAGGAGCTT CCCTGAGTGT 720
GAACTGGAAA TCCATTTCCC CTCACCAGGA ACTGACTGAC TTGAACATGA GCACGTGATG 780
CAATTCTGGC CAGGAAGACT CGGGACAAAG TCCACCCATG GCTCCAAGAA AAGATGTGCA 840
TCTGATAAAG AGCAAGCCAA ACAGACAAGA CACATAGATG CCCTCTTTTT CTTCTTTGAG 900
ATTTTGTTTG GATGTGACAC CTGGAGCTGC TGCAGCCATT 940
|
