Variant report
| Variant | rs7708947 |
|---|---|
| Chromosome Location | chr5:112711076-112711077 |
| allele | C/T |
| Outlinks | Ensembl UCSC |
| No. | Chromosome Location | Chromatin state | Cell line | Tissue |
|---|---|---|---|---|
| 1 | chr5:112700800-112718000 | Weak transcription | Foreskin Keratinocyte Primary Cells skin03 | Skin |
| 2 | chr5:112707800-112719000 | Weak transcription | Mesenchymal Stem Cell Derived Adipocyte Cultured Cells | ES cell derived |
| 3 | chr5:112708000-112713800 | Weak transcription | HMEC | breast |
| 4 | chr5:112708000-112714000 | Weak transcription | NHEK | skin |
| 5 | chr5:112708000-112716200 | Weak transcription | Fetal Kidney | kidney |
| 6 | chr5:112708600-112711200 | Weak transcription | Fetal Stomach | stomach |
| 7 | chr5:112708600-112713400 | Weak transcription | HUVEC | blood vessel |
| 8 | chr5:112708800-112711200 | Weak transcription | Breast variant Human Mammary Epithelial Cells (vHMEC) | Breast |
| 9 | chr5:112710600-112714200 | Weak transcription | IMR90 fetal lung fibroblasts Cell Line | lung |
| 10 | chr5:112711000-112713200 | Enhancers | Dnd41 | blood |
