Variant report
Variant | rs72965321 |
---|---|
Chromosome Location | chr6:117709381-117709382 |
allele | C/T |
Outlinks | Ensembl   UCSC |
No. | Chromosome Location | Chromatin state | Cell line | Tissue |
---|---|---|---|---|
1 | chr6:117662000-117717200 | Weak transcription | HSMMtube | muscle |
2 | chr6:117692600-117735800 | Weak transcription | Bone Marrow Derived Cultured Mesenchymal Stem Cells | Bone marrow |
3 | chr6:117692800-117717400 | Weak transcription | Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells | embryonic stem cell |
4 | chr6:117707000-117709600 | Enhancers | Stomach Mucosa | stomach |
5 | chr6:117707400-117715800 | Weak transcription | HSMM | muscle |
6 | chr6:117708000-117714200 | Enhancers | Liver | Liver |
7 | chr6:117708600-117709600 | Enhancers | A549 | lung |
8 | chr6:117708800-117709400 | Genic enhancers | Breast variant Human Mammary Epithelial Cells (vHMEC) | Breast |
9 | chr6:117708800-117709400 | Enhancers | Pancreas | Pancrea |
10 | chr6:117708800-117710600 | Enhancers | HMEC | breast |
11 | chr6:117708800-117713000 | Enhancers | Fetal Intestine Large | intestine |
12 | chr6:117709000-117709400 | Enhancers | Gastric | stomach |
13 | chr6:117709000-117712200 | Enhancers | HepG2 | liver |
14 | chr6:117709200-117711600 | Enhancers | Fetal Intestine Small | intestine |