Variant report
| Variant | rs2166383 |
|---|---|
| Chromosome Location | chr5:16496211-16496212 |
| allele | C/T |
| Outlinks | Ensembl UCSC |
| No. | Chromosome Location | Chromatin state | Cell line | Tissue |
|---|---|---|---|---|
| 1 | chr5:16488400-16499800 | Weak transcription | Gastric | stomach |
| 2 | chr5:16492200-16499600 | Weak transcription | Right Ventricle | heart |
| 3 | chr5:16494400-16497200 | ZNF genes & repeats | Fetal Intestine Small | intestine |
| 4 | chr5:16494400-16497200 | Enhancers | Psoas Muscle | Psoas |
| 5 | chr5:16494600-16497400 | ZNF genes & repeats | Primary T cells from cord blood | blood |
| 6 | chr5:16494800-16496400 | Enhancers | Skeletal Muscle Male | skeletal muscle |
| 7 | chr5:16495200-16497200 | Weak transcription | Fetal Heart | heart |
| 8 | chr5:16495800-16497600 | Strong transcription | Breast variant Human Mammary Epithelial Cells (vHMEC) | Breast |
| 9 | chr5:16495800-16504400 | Weak transcription | Rectal Mucosa Donor 29 | rectum |
| 10 | chr5:16495800-16509000 | Weak transcription | H1 Derived Mesenchymal Stem Cells | ES cell derived |
| 11 | chr5:16496000-16496400 | Enhancers | Skeletal Muscle Female | skeletal muscle |
| 12 | chr5:16496200-16509000 | Weak transcription | iPS DF 6.9 Cell Line | embryonic stem cell |
