Variant report
| Variant | rs1976058 |
|---|---|
| Chromosome Location | chr2:111792734-111792735 |
| allele | C/T |
| Outlinks | Ensembl UCSC |
| No. | Chromosome Location | Chromatin state | Cell line | Tissue |
|---|---|---|---|---|
| 1 | chr2:111786000-111795800 | Enhancers | Primary monocytes fromperipheralblood | blood |
| 2 | chr2:111786800-111792800 | Enhancers | Fetal Intestine Small | intestine |
| 3 | chr2:111787000-111792800 | Enhancers | Fetal Intestine Large | intestine |
| 4 | chr2:111787400-111795600 | Weak transcription | H1 Cell Line | embryonic stem cell |
| 5 | chr2:111787800-111825400 | Weak transcription | ES-UCSF4 Cell Line | embryonic stem cell |
| 6 | chr2:111788200-111793400 | Weak transcription | Fetal Thymus | thymus |
| 7 | chr2:111788200-111799200 | Weak transcription | iPS DF 19.11 Cell Line | embryonic stem cell |
| 8 | chr2:111790800-111793600 | Weak transcription | Primary Natural Killer cells fromperipheralblood | blood |
| 9 | chr2:111790800-111799200 | Weak transcription | H1 Derived Neuronal Progenitor Cultured Cells | ES cell derived |
| 10 | chr2:111790800-111800200 | Weak transcription | Spleen | Spleen |
| 11 | chr2:111791200-111794600 | Weak transcription | Breast variant Human Mammary Epithelial Cells (vHMEC) | Breast |
| 12 | chr2:111791200-111795600 | Weak transcription | Gastric | stomach |
| 13 | chr2:111791200-111795800 | Enhancers | Monocytes-CD14+_RO01746 | blood |
| 14 | chr2:111791400-111793400 | Weak transcription | Primary B cells from cord blood | blood |
| 15 | chr2:111792200-111793000 | Enhancers | Fetal Kidney | kidney |
| 16 | chr2:111792400-111796600 | Weak transcription | Fetal Lung | lung |
| 17 | chr2:111792400-111797200 | Weak transcription | Fetal Heart | heart |
