| Tag | Content |
|---|
EnhancerAtlas ID | HS184-19503 |
Organism | Homo sapiens |
Tissue/cell | T47D |
Coordinate | chr22:41398940-41399560 |
TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| EHF | MA0598.2 | chr22:41399200-41399212 | AACCCGGAAGTA | + | 7.22 | | ELF1 | MA0473.2 | chr22:41399200-41399212 | AACCCGGAAGTA | + | 6.92 | | ELF3 | MA0640.1 | chr22:41399200-41399213 | AACCCGGAAGTAC | + | 6.78 | | ELF4 | MA0641.1 | chr22:41399200-41399212 | AACCCGGAAGTA | + | 6.92 | | ELF5 | MA0136.2 | chr22:41399201-41399212 | ACCCGGAAGTA | + | 6.62 |
|
| | 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 |
| GH22I041000 | chr22 | 41396302 | 41399943 |
|
Enhancer Sequence | ACACCTCCTT TGCAGGGTGA GGCTCTGGAT TTAGGGCACG TGCTATAGAA ATGTTAGTTT 60
CCTTCCTCCT AACCCTGGCT CAGCCATTTA CTGGCTCTGT GGCCTGGGAG AAGGTCTTTA 120
CCTTCTTGGA GCTTCTGTTT CCTCATAGGT ATCTCTAAAG TCGCTTCTAC ACCTGGGAGC 180
CTTGGGCCCT GATGGGTTAA ATATGGAAGC TCTGAGAAGC CAGGTTGGCT GCTCCAGCTC 240
CTTCCTTCCC AACCAAAACA AACCCGGAAG TACAGGTTCT TTCTGATGAC AGCAACCCCC 300
AGCCACAGGT TTTCCAGGGC TGGGCTAATT TCAGACGAGA ATCCCGTGCT TGTCAGACCA 360
GATTTCCTGC TTTGGGACTT GGGAAATCCA GTTGCCTTAA ACTGACCTTT CTCTGGGCCA 420
CTCTTCTTGT ACCAGGTGGA GAACCTGTAG CAAAAAAAAA AAAACTGGTC ACAGTCCGTA 480
GACCCACGGC CTCGTAGAGA ACGGCAGTGG GAGTCACGAC ATCGTGCTGG GTCCCAGGGA 540
CCTGGTGTTA AGTTCTCCAT GGAGCTTTCT GTTTTTCTTT CTTTCTTTTT ATAATTGAGG 600
TGAAATTCAC ATAACAGAAA 620
|
