| Tag | Content |
|---|
EnhancerAtlas ID | HS098-28114 |
Organism | Homo sapiens |
Tissue/cell | HSMM |
Coordinate | chr19:45188110-45188800 |
SNPs | | Number: 1 | ID | Chromosome | Position | Genome Version |
|
TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| HSF1 | MA0486.2 | chr19:45188681-45188694 | GAAACTTCTAGAA | - | 6.25 | | ZNF263 | MA0528.1 | chr19:45188201-45188222 | GGTGGAGAGGGTGGGGAAGGA | + | 6.04 | | ZNF263 | MA0528.1 | chr19:45188213-45188234 | GGGGAAGGAGGAAAAGGTGGG | + | 6.16 | | ZNF263 | MA0528.1 | chr19:45188216-45188237 | GAAGGAGGAAAAGGTGGGTGG | + | 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 |
| GH19I044683 | chr19 | 45186982 | 45190472 |
|
Enhancer Sequence | AAGATCGTGC CCCTGCACTC CAGCCTGGGT GACAGAGCAA GACTCCACCT CAAAAAAAAA 60
AAAAAAAAAG GAGCAGCAAG GAGGCCAGTG TGGTGGAGAG GGTGGGGAAG GAGGAAAAGG 120
TGGGTGGAAG TTGACGTCAG GAGATGGACG GAGGGGCACA TGGCGCAGGG CCAGGTAAGG 180
CACTGCCGAG ACTGTGGCTT TGAGGGGCAG GGTGCTGTGA AAGGCGAATA ACGGCCCCCC 240
AGTGACGTCT ACATCCTAAT CCCCTGTGAA TGTTACGTTA TATGACAAAA GAATGCAGCC 300
ATGATTAAGT TCAGGATCGT GCTTTGGGGA GATTATCCTG GATTGCCCTG GCAGGCTCTT 360
TATGTAATCA CACAGATCCT TATAATCGAG AAGGACACAG GAAGCGTGAG TCAGAGGGGC 420
TGTGACAACA AAGGAAGCAA AGCCCTTTGA AGACGGGAGA AGGAGCTGAA AGTCAAGCAG 480
CACTTCAGAG TCAGAATGAT TGAGTGTGAG AGAGTCCATG GGCCATCGTG AGTGTTGAAG 540
ACGGAAGGGG GCCTTGAGCT AAGGAATGCA AGAAACTTCT AGAAGCTGGA GGAGGGCCAA 600
GCTCAGTGGC TCACGCCTGC AGTCCCAGCA CTTTGGGAGG CCAAGGTGGG AGGATCGCTT 660
GAGGCCAGGA GTTGGAGACC AGCCTGGGCA 690
|
