Variant report
| Variant | rs11580993 |
|---|---|
| Chromosome Location | chr1:153339314-153339315 |
| allele | A/C |
| Outlinks | Ensembl UCSC |
| No. | Chromosome Location | Chromatin state | Cell line | Tissue |
|---|---|---|---|---|
| 1 | chr1:153332600-153340000 | Weak transcription | Spleen | Spleen |
| 2 | chr1:153333600-153346200 | Enhancers | Primary monocytes fromperipheralblood | blood |
| 3 | chr1:153333800-153341400 | Enhancers | Placenta | Placenta |
| 4 | chr1:153334000-153339600 | Flanking Active TSS | Primary neutrophils fromperipheralblood | blood |
| 5 | chr1:153334800-153339400 | Enhancers | Esophagus | oesophagus |
| 6 | chr1:153335600-153341400 | Flanking Active TSS | Monocytes-CD14+_RO01746 | blood |
| 7 | chr1:153336000-153339400 | Enhancers | Fetal Thymus | thymus |
| 8 | chr1:153338200-153343200 | Weak transcription | HMEC | breast |
| 9 | chr1:153338200-153343400 | Weak transcription | Foreskin Keratinocyte Primary Cells skin03 | Skin |
| 10 | chr1:153338400-153340000 | Weak transcription | Breast variant Human Mammary Epithelial Cells (vHMEC) | Breast |
| 11 | chr1:153338400-153340400 | Weak transcription | Fetal Intestine Small | intestine |
| 12 | chr1:153338400-153343200 | Weak transcription | NHEK | skin |
| 13 | chr1:153338400-153343600 | Weak transcription | Foreskin Keratinocyte Primary Cells skin02 | Skin |
| 14 | chr1:153338600-153340000 | Weak transcription | Fetal Intestine Large | intestine |
| 15 | chr1:153339000-153340400 | Weak transcription | Primary Natural Killer cells fromperipheralblood | blood |
| 16 | chr1:153339200-153339400 | Flanking Active TSS | Primary B cells from cord blood | blood |
| 17 | chr1:153339200-153339600 | Enhancers | Brain Hippocampus Middle | brain |
