Variant report
| Variant | rs3916061 |
|---|---|
| Chromosome Location | chr17:38127713-38127714 |
| allele | A/G |
| Outlinks | Ensembl UCSC |
| No. | Chromosome Location | Chromatin state | Cell line | Tissue |
|---|---|---|---|---|
| 1 | chr17:38110800-38128800 | Weak transcription | Gastric | stomach |
| 2 | chr17:38122200-38130600 | Weak transcription | iPS DF 19.11 Cell Line | embryonic stem cell |
| 3 | chr17:38122200-38130600 | Enhancers | Primary monocytes fromperipheralblood | blood |
| 4 | chr17:38124000-38128000 | Weak transcription | Primary hematopoietic stem cells | blood |
| 5 | chr17:38124000-38129600 | Weak transcription | Breast variant Human Mammary Epithelial Cells (vHMEC) | Breast |
| 6 | chr17:38124000-38134600 | Weak transcription | Foreskin Keratinocyte Primary Cells skin02 | Skin |
| 7 | chr17:38125200-38128400 | Weak transcription | Primary B cells from cord blood | blood |
| 8 | chr17:38125400-38128000 | Enhancers | Colonic Mucosa | Colon |
| 9 | chr17:38126200-38127800 | Enhancers | Placenta | Placenta |
| 10 | chr17:38126400-38128000 | Weak transcription | Primary neutrophils fromperipheralblood | blood |
| 11 | chr17:38126800-38128000 | Enhancers | Monocytes-CD14+_RO01746 | blood |
| 12 | chr17:38127000-38128000 | Strong transcription | Foreskin Keratinocyte Primary Cells skin03 | Skin |
| 13 | chr17:38127400-38128200 | Bivalent Enhancer | Fetal Adrenal Gland | Adrenal Gland |
| 14 | chr17:38127400-38129200 | Bivalent Enhancer | Primary hematopoietic stem cells short term culture | blood |
| 15 | chr17:38127600-38127800 | Flanking Active TSS | K562 | blood |
| 16 | chr17:38127600-38128200 | Bivalent Enhancer | Fetal Thymus | thymus |
