| Tag | Content |
|---|
EnhancerAtlas ID | HS093-11537 |
Organism | Homo sapiens |
Tissue/cell | HL-60 |
Coordinate | chr16:27771070-27771700 |
TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| BHLHE40 | MA0464.2 | chr16:27771088-27771098 | ATCACGTGAC | + | 6.02 | | MITF | MA0620.2 | chr16:27771084-27771102 | GCAAATCACGTGACCCAG | + | 6.08 | | MITF | MA0620.2 | chr16:27771084-27771102 | GCAAATCACGTGACCCAG | - | 6.08 | | TFEB | MA0692.1 | chr16:27771088-27771098 | ATCACGTGAC | + | 6.02 | | USF2 | MA0526.2 | chr16:27771086-27771102 | AAATCACGTGACCCAG | - | 6.24 |
|
| | 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 |
| GH16I027759 | chr16 | 27770334 | 27772150 |
|
Enhancer Sequence | TCCCAGTGTT CAAAGCAAAT CACGTGACCC AGAGTCAGGA GCAGAGAAGG AAACTCCAAC 60
TCTGGATGGG ATGAGGGGCA AAATCACATT GCAACAGCAG GGACACGGGA TGGGACGAGC 120
TTGTAGCCAC TTTGCACGTG AATGATGCGG CGAGAAGCCC ATGTGCAGGG TGCCGTGCTG 180
GCCACATGTT TTTTTCATCT GCCCCAGAGA TGCTCAGAGT TACCTTGGCA CCACGAAGGA 240
GGAAAAGGAT CTGAGGGCTA AGTTACAAAA AGTATGTTGG GAGATGTCAG GGGCGTGGGA 300
GAGAAAACCA AGCTCCAGGG AGGTCAGGTG ACCCAGCCCC TCTTCATGGC CACAAAGAAG 360
TCCTTTCACC TCTCTGGGCT TCCAGTTCCT CATCTGAGCT GCAAGGGGGT GGTGCCAGAT 420
GACACCCTGC TTCCTTCTGC CTGCTCTGTG GTGCTGGCAT TTCTGTGAAC GCTGCAAAGA 480
GTGAGTCTTA CACTTAGCTA CCCAAAAGGG TGCTAAAATA TGCGGCAAAT TCTCTAAGGG 540
CAGAAGGGTT TATTGTGTTT GGTCTTGCTC TAATGAGACA CCGTTAAGGA AAGAGACGTT 600
CCAGCCAATT ATCTGACAGG GCTTGATCAA 630
|
