Variant report
Variant | rs17079119 |
---|---|
Chromosome Location | chr6:117713312-117713313 |
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 | chr6:117707400-117715800 | Weak transcription | HSMM | muscle |
5 | chr6:117708000-117714200 | Enhancers | Liver | Liver |
6 | chr6:117709600-117713800 | Weak transcription | Stomach Mucosa | stomach |
7 | chr6:117711400-117714000 | Weak transcription | Foreskin Keratinocyte Primary Cells skin02 | Skin |
8 | chr6:117711600-117713800 | Weak transcription | Breast variant Human Mammary Epithelial Cells (vHMEC) | Breast |
9 | chr6:117711600-117713800 | Weak transcription | Foreskin Keratinocyte Primary Cells skin03 | Skin |
10 | chr6:117711600-117714000 | Weak transcription | NHEK | skin |
11 | chr6:117712600-117713800 | Enhancers | HepG2 | liver |
12 | chr6:117713000-117713400 | Weak transcription | HMEC | breast |