Variant report
Variant | rs17318858 |
---|---|
Chromosome Location | chr11:10579687-10579688 |
allele | C/T |
Outlinks | Ensembl   UCSC |
No. | Chromosome Location | Chromatin state | Cell line | Tissue |
---|---|---|---|---|
1 | chr11:10573000-10603200 | Weak transcription | Breast variant Human Mammary Epithelial Cells (vHMEC) | Breast |
2 | chr11:10575000-10580200 | Weak transcription | Aorta | Aorta |
3 | chr11:10576000-10585800 | Weak transcription | Placenta | Placenta |
4 | chr11:10576200-10583600 | Weak transcription | Spleen | Spleen |
5 | chr11:10578200-10583800 | Weak transcription | Primary B cells from peripheral blood | blood |
6 | chr11:10578200-10590000 | Weak transcription | ES-I3 Cell Line | embryonic stem cell |
7 | chr11:10578400-10580000 | Strong transcription | Fetal Adrenal Gland | Adrenal Gland |
8 | chr11:10578600-10580600 | Enhancers | Fetal Intestine Small | intestine |
9 | chr11:10578600-10585400 | Weak transcription | Fetal Stomach | stomach |
10 | chr11:10578800-10580000 | Weak transcription | Small Intestine | intestine |
11 | chr11:10579200-10581400 | Weak transcription | Primary B cells from cord blood | blood |
12 | chr11:10579400-10579800 | Weak transcription | Fetal Intestine Large | intestine |
13 | chr11:10579400-10581200 | Weak transcription | Adipose Nuclei | Adipose |