Variant report
Variant | rs207441 |
---|---|
Chromosome Location | chr2:31563014-31563015 |
allele | G/T |
Outlinks | Ensembl   UCSC |
No. | Chromosome Location | Chromatin state | Cell line | Tissue |
---|---|---|---|---|
1 | chr2:31548000-31634600 | Weak transcription | Pancreatic Islets | Pancreatic Islet |
2 | chr2:31557200-31579600 | Strong transcription | Liver | Liver |
3 | chr2:31557600-31563600 | Weak transcription | Gastric | stomach |
4 | chr2:31558200-31573200 | Strong transcription | Fetal Intestine Large | intestine |
5 | chr2:31558800-31564600 | Strong transcription | Fetal Intestine Small | intestine |
6 | chr2:31559600-31565600 | Strong transcription | Duodenum Mucosa | Duodenum |
7 | chr2:31560400-31576800 | Weak transcription | Sigmoid Colon | Sigmoid Colon |
8 | chr2:31560800-31570800 | Weak transcription | H1 Derived Mesenchymal Stem Cells | ES cell derived |
9 | chr2:31560800-31599800 | Weak transcription | Esophagus | oesophagus |
10 | chr2:31561200-31569800 | Weak transcription | Foreskin Fibroblast Primary Cells skin02 | Skin |
11 | chr2:31561400-31564200 | Weak transcription | IMR90 fetal lung fibroblasts Cell Line | lung |
12 | chr2:31561600-31563600 | Weak transcription | Breast Myoepithelial Primary Cells | Breast |
13 | chr2:31561600-31570400 | Weak transcription | NHLF | lung |
14 | chr2:31562000-31564000 | Weak transcription | Foreskin Fibroblast Primary Cells skin01 | Skin |
15 | chr2:31562200-31564000 | Strong transcription | Foreskin Keratinocyte Primary Cells skin03 | Skin |
16 | chr2:31562400-31563800 | Strong transcription | NHEK | skin |
17 | chr2:31562400-31564000 | Strong transcription | HMEC | breast |
18 | chr2:31562600-31563800 | Weak transcription | Breast variant Human Mammary Epithelial Cells (vHMEC) | Breast |
19 | chr2:31562800-31563800 | Strong transcription | Foreskin Keratinocyte Primary Cells skin02 | Skin |
20 | chr2:31562800-31563800 | Weak transcription | Placenta | Placenta |