Variant report
Variant | rs7000889 |
---|---|
Chromosome Location | chr8:42547582-42547583 |
allele | A/G |
Outlinks | Ensembl   UCSC |
No. | Chromosome Location | Chromatin state | Cell line | Tissue |
---|---|---|---|---|
1 | chr8:42544000-42561200 | Weak transcription | H1 Derived Neuronal Progenitor Cultured Cells | ES cell derived |
2 | chr8:42545200-42547800 | Weak transcription | HSMM | muscle |
3 | chr8:42546400-42547600 | Weak transcription | HUES6 Cell Line | embryonic stem cell |
4 | chr8:42546800-42547800 | Weak transcription | HepG2 | liver |
5 | chr8:42547200-42547800 | Enhancers | iPS DF 19.11 Cell Line | embryonic stem cell |
6 | chr8:42547200-42548000 | Enhancers | Foreskin Fibroblast Primary Cells skin02 | Skin |
7 | chr8:42547400-42548000 | Enhancers | Adipose Nuclei | Adipose |
8 | chr8:42547400-42548000 | Enhancers | Dnd41 | blood |
9 | chr8:42547400-42548200 | Enhancers | Foreskin Keratinocyte Primary Cells skin03 | Skin |
10 | chr8:42547400-42548400 | Enhancers | Primary T killer memory cells from peripheral blood | blood |
11 | chr8:42547400-42548400 | Enhancers | Foreskin Fibroblast Primary Cells skin01 | Skin |
12 | chr8:42547400-42548600 | Enhancers | iPS DF 6.9 Cell Line | embryonic stem cell |