Variant report
Variant | rs10163436 |
---|---|
Chromosome Location | chr16:70665518-70665519 |
allele | C/T |
Outlinks | Ensembl   UCSC |
No. | Chromosome Location | Chromatin state | Cell line | Tissue |
---|---|---|---|---|
1 | chr16:70647400-70669200 | Weak transcription | Right Atrium | heart |
2 | chr16:70659200-70668800 | Weak transcription | iPS-15b Cell Line | embryonic stem cell |
3 | chr16:70661200-70669000 | Weak transcription | Foreskin Fibroblast Primary Cells skin02 | Skin |
4 | chr16:70663000-70666400 | Weak transcription | Foreskin Keratinocyte Primary Cells skin03 | Skin |
5 | chr16:70663000-70669000 | Weak transcription | Breast variant Human Mammary Epithelial Cells (vHMEC) | Breast |
6 | chr16:70663400-70668800 | Weak transcription | ES-UCSF4 Cell Line | embryonic stem cell |
7 | chr16:70665000-70665600 | ZNF genes & repeats | ES-I3 Cell Line | embryonic stem cell |
8 | chr16:70665200-70668800 | Weak transcription | HUES6 Cell Line | embryonic stem cell |
9 | chr16:70665200-70669000 | Weak transcription | Breast Myoepithelial Primary Cells | Breast |
10 | chr16:70665400-70665600 | Enhancers | NHLF | lung |
11 | chr16:70665400-70669200 | Weak transcription | H1 Derived Mesenchymal Stem Cells | ES cell derived |
12 | chr16:70665400-70669200 | Weak transcription | Fetal Intestine Small | intestine |