| Tag | Content |
|---|
EnhancerAtlas ID | HS108-12523 |
Organism | Homo sapiens |
Tissue/cell | K562 |
Coordinate | chr14:93192090-93193490 |
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 | TTGTATTTTA GTAGAGATGG GGTTTCACCA TGTTGGCCAG GCTGGTCTCA AACTCCTGAC 60
CTCAGGTGAT CCACCTACCT TGGTCTCCCA AAGTGATGAA ATTACAGGTG TGAGCCACCA 120
CACCTGGCCA CGGATTTTTT TAAATATAAA AGTGATATTG TGCAACAACA TGGATTAATC 180
TCAAAACACC ATAAGTTATG AGCTCATCTG ACCGGGCACA GTGGCTCATA CCTGTAATCC 240
CAGCACTTTG GGAGGCTGAG GCAGGTGGAT CATCAGAGGT CAGGAGATCG AGACCAGTCT 300
GGCTAACATG GTAAAACCCT GTCTCTACTA AAAATACAAA AATTAGCCGG GCGTGGTGGC 360
AGGTGCCTGT AATCCCAGCT ATTCGGGAGG CTGAGACAGG AGAATCGCTT AAACCCAGGA 420
GGCGGAGACT GCAGTGAGCT GAGATCACGC CATTGCACTC CAGGCTGGGC AACAAGATTG 480
AGGCTCTGTC TCAAAAAAAA AAAAAAAATT AAATAAGTAA ACAAATAGCT TGTGAGAAAC 540
AGACTGTGAG TCACCACCAC CTCCTTCCTG CACTCCCTGG CCACTCCCTC TCGCCTCCGT 600
CACTGCAGTC TGCCCAGCCT GTCTTTGGCC CCGCCAGCCT CGATTTTTGC CCCTTGGCCC 660
ACAAAACCTC AAATATCTAC TATCTGGCCC TTTATAGAAA AAAACTCTGC AGGCCCCAGT 720
CTTGAGCCAG ACAGCAATGG TGAGGCTCTG AGTGTGTGGG GGTGGGGAAG GGGCTTGCCA 780
GGAGCACACA GAGTGAGGAG CTCCCTGTTC TTGTCATTGG TGACATGGCG CCTGTCCAAC 840
CCTTTATCTA CTTCTGAGTG GAGAGGTTCT GTCAAAGGGA AAGAAAGGGA GAGTTGCTGA 900
CTGGGCCTTC TCCTCCTAAC ACGCCTCACC ATGCCCTCAC CCTACCTTGC CGGTCTCCTT 960
CTCCCTCGCT TCCTCCTCCC CATCTACCTG GGCCATGCAC TGTCCTTGCA TGCCCTGTGG 1020
CCACCTTCCT TTCCACCAGG GCCCTGGCTT TGCTCAGATG ACCTACCCAG CTCCAAGTGG 1080
TCACAAGTGG TCAGGAGCTT CCCTGAGTGT GAACTGGAAA TCCATTTCCC CTCACCAGGA 1140
ACTGACTGAC TTGAACATGA GCACGTGATG CAATTCTGGC CAGGAAGACT CGGGACAAAG 1200
TCCACCCATG GCTCCAAGAA AAGATGTGCA TCTGATAAAG AGCAAGCCAA ACAGACAAGA 1260
CACATAGATG CCCTCTTTTT CTTCTTTGAG ATTTTGTTTG GATGTGACAC CTGGAGCTGC 1320
TGCAGCCATT TCGTGACTAT GAGGAGAGTG TATTTGAGGA CAGTTCGTCA CAACTATGAT 1380
GACAGAGTAG CAAGATGAAA 1400
|
