Variant report
| Variant | rs5029891 |
|---|---|
| Chromosome Location | chr1:172451759-172451760 |
| allele | G/T |
| Outlinks | Ensembl UCSC |
| No. | Chromosome Location | Chromatin state | Cell line | Tissue |
|---|---|---|---|---|
| 1 | chr1:172444200-172456200 | Weak transcription | Monocytes-CD14+_RO01746 | blood |
| 2 | chr1:172445000-172452400 | Weak transcription | Primary neutrophils fromperipheralblood | blood |
| 3 | chr1:172447600-172452800 | Weak transcription | hESC Derived CD56+ Mesoderm Cultured Cells | ES cell derived |
| 4 | chr1:172448200-172452600 | Weak transcription | Breast variant Human Mammary Epithelial Cells (vHMEC) | Breast |
| 5 | chr1:172448200-172452800 | Weak transcription | Foreskin Keratinocyte Primary Cells skin02 | Skin |
| 6 | chr1:172448400-172452800 | Weak transcription | HMEC | breast |
| 7 | chr1:172448600-172453200 | Weak transcription | Foreskin Keratinocyte Primary Cells skin03 | Skin |
| 8 | chr1:172448600-172453200 | Weak transcription | NHEK | skin |
| 9 | chr1:172449800-172453000 | Weak transcription | Placenta | Placenta |
| 10 | chr1:172450000-172452800 | Weak transcription | Breast Myoepithelial Primary Cells | Breast |
| 11 | chr1:172450200-172456200 | Weak transcription | Primary T cells from cord blood | blood |
| 12 | chr1:172450800-172452600 | Enhancers | Fetal Intestine Large | intestine |
| 13 | chr1:172450800-172456400 | Enhancers | Placenta Amnion | Placenta Amnion |
| 14 | chr1:172451000-172452000 | Enhancers | Fetal Intestine Small | intestine |
| 15 | chr1:172451600-172452400 | Weak transcription | HepG2 | liver |
| 16 | chr1:172451600-172452600 | Weak transcription | A549 | lung |
| 17 | chr1:172451600-172453000 | Enhancers | H1 BMP4 Derived Trophoblast Cultured Cells | ES cell derived |
| 18 | chr1:172451600-172453000 | Enhancers | H1 Derived Mesenchymal Stem Cells | ES cell derived |
