Variant report
| Variant | rs9508613 |
|---|---|
| Chromosome Location | chr13:30581123-30581124 |
| allele | A/T |
| Outlinks | Ensembl UCSC |
| No. | Chromosome Location | Chromatin state | Cell line | Tissue |
|---|---|---|---|---|
| 1 | chr13:30577800-30581200 | Enhancers | Primary neutrophils fromperipheralblood | blood |
| 2 | chr13:30578800-30583000 | Weak transcription | Breast variant Human Mammary Epithelial Cells (vHMEC) | Breast |
| 3 | chr13:30578800-30588200 | Weak transcription | Placenta Amnion | Placenta Amnion |
| 4 | chr13:30580200-30581200 | Enhancers | Primary T cells from cord blood | blood |
| 5 | chr13:30580400-30581600 | Enhancers | H1 BMP4 Derived Mesendoderm Cultured Cells | ES cell derived |
| 6 | chr13:30580800-30586800 | Weak transcription | H1 BMP4 Derived Trophoblast Cultured Cells | ES cell derived |
| 7 | chr13:30581000-30581200 | Enhancers | Foreskin Fibroblast Primary Cells skin01 | Skin |
| 8 | chr13:30581000-30592000 | Weak transcription | HUES6 Cell Line | embryonic stem cell |
