| Tag | Content |
|---|
EnhancerAtlas ID | HS089-09615 |
Organism | Homo sapiens |
Tissue/cell | Hela |
Coordinate | chr4:1289380-1290080 |
TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| ZNF263 | MA0528.1 | chr4:1289823-1289844 | CCCCTCACCTGCTCCTCCCTC | - | 6.09 | | ZNF263 | MA0528.1 | chr4:1290024-1290045 | CCCCTCACCTGCTCCTCCCTC | - | 6.09 | | ZNF263 | MA0528.1 | chr4:1289838-1289859 | TCCCTCACCTGCTCCTCCCTC | - | 6.17 | | ZNF263 | MA0528.1 | chr4:1290039-1290060 | TCCCTCACCTGCTCCTCCCTC | - | 6.17 | | ZNF263 | MA0528.1 | chr4:1289820-1289841 | GCCCCCCTCACCTGCTCCTCC | - | 6.28 | | ZNF263 | MA0528.1 | chr4:1290021-1290042 | GCCCCCCTCACCTGCTCCTCC | - | 6.28 | | ZNF263 | MA0528.1 | chr4:1289835-1289856 | TCCTCCCTCACCTGCTCCTCC | - | 7.59 | | ZNF263 | MA0528.1 | chr4:1290036-1290057 | TCCTCCCTCACCTGCTCCTCC | - | 7.59 |
|
| | 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 |
| GH04I001293 | chr4 | 1287628 | 1289506 |
|
Enhancer Sequence | ACCTGCACCT GCTCCCACAC CCGTGGTGGA TGAGCCCCAT CACCCGTACC TGTACCCCCC 60
TCACCCGCTC CTGTACCCCC TCACCCGCTC CTATACCCCC TCACCCACAC CTGTACCCCC 120
CTCACCCGCT CCTGTACCCC CTCACCCGCG CCTGTGCCCC CTCACCCGTG CCTCTGCCCC 180
CCTCACCCGC GCCTGTGCCC CCCTCCCCAG CGCCTGTGCC CCCTCACCCA CGCCTGTGCC 240
CTCCTCACCC ATGCCGGTGC CCACCACACC TGCGCCTTTG CCCCTTCACC TGTGTCTGCA 300
CCGCCCTCAC CTGTGCTGCC TTCACCTGCA CCCCCTCACC CACACCTGTG CCACCCTCGC 360
CCGCACCTGT GCCCCCCTCA CCCACGTCTG CACTGCCCTC ACCTGTGCTG CCCTCACCTG 420
TGCCCCCCAC CTGTGCCTGT GCCCCCCTCA CCTGCTCCTC CCTCACCTGC TCCTCCCTCA 480
CCTGCTCCTG CACCACCTTC ACGTGCGCCC CCCACCTACA TCTGCACCTC ACCTATGCTA 540
CCCTCACCTG TGCCCCCCCA CCCGCACCTG TGCCCCCCTC ACCCACGTCT GCACTGCCCT 600
CACCTGTGCT GCCCTCACCT GTGCCCCCCA CCTGTGCCTG TGCCCCCCTC ACCTGCTCCT 660
CCCTCACCTG CTCCTCCCTC ACCTGCTCCT GCACCACCTT 700
|
