| Tag | Content |
|---|
EnhancerAtlas ID | HS183-01536 |
Organism | Homo sapiens |
Tissue/cell | T47D-MTVL |
Coordinate | chr14:105242140-105242990 |
TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| ZNF740 | MA0753.2 | chr14:105242414-105242427 | CCGCCCCCCCCAA | + | 6.54 |
|
| | 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 |
| GH14I104773 | chr14 | 105240305 | 105242303 |
|
Enhancer Sequence | AGGAGGTCAG GTGAGGCTGC AGGCCTGTAC CAGATCAGGA GCTCCACCCC ACGTCTTTCA 60
CCCACCCGCC AGCCTCACAA GCGTGGTTCC ACAGCTGTCG GGGTTCCCAG AGACAGCCCT 120
GAGGAGGCCA CCACTTGACC TGGTCTGGCC ACATACACTC AGGGTCACGA AGCCCTCTTG 180
GACGTGGGGG ACACCCAGGC TTAGCCCCCC AGCAGGACTC TGTCCCCACA ACCGGACTCC 240
AACCCCCAGC AGGACTCCGC CCCCCAGCAG GACTCCGCCC CCCCCAAGCA GGACTCCGCC 300
TCCCAAGCAG GACTCCGCCC CCCAAGGAGG ACTGGCCCTC TCCACCGGGT TTTTCTTTTT 360
TTGAGACGGA GTCTTGCTCT ATCGCCCTGG CTGGAGTGCA GTGGTAAAAT CTCGGCTCCT 420
GCAGCCTCTG CCTCTCGGGT TCAAGCGATT CTTGTGCCTC AGCCTCCCAA GTAGCCGGGA 480
TTACAGGTGT GCACCACCAC ACCCAGCTAA GTTTTATATT TTTAGTAGAG ACGGGGGTTT 540
CACCATGTTG GCAGGCTAGT CTCAAACTCC TGGTCTCAAG TGATCTGCGC ACCTCGGCCT 600
CCCAAAGTGC CGAGATTATA GACGTGAGCC ACTGCACCCG GTCCCTAGCC AGTTTTTATC 660
TCCAGCCTCA GTTTCCCCAC CCAAACCCCA CAGGCAGGAC TGGGCCAGTT TCCAAACTGG 720
GCTCTGAGGA GGGCCTGGGA GCACTGGGGA GTGAGGATGG CTACAGGCAG AGGTGCCAGC 780
ACCCCGCCAT CCCCGTGTCC CTCCTAAGCG CTGGGGCTGC CCAAGTGCCT GGCCTGGCCG 840
CCACAGCCCA 850
|
