Variant report
| Variant | rs999157 |
|---|---|
| Chromosome Location | chr1:59181597-59181598 |
| allele | G/T |
| Outlinks | Ensembl UCSC |
| No. | Chromosome Location | Chromatin state | Cell line | Tissue |
|---|---|---|---|---|
| 1 | chr1:59166400-59186200 | Weak transcription | Foreskin Keratinocyte Primary Cells skin03 | Skin |
| 2 | chr1:59176000-59182800 | Weak transcription | HUVEC | blood vessel |
| 3 | chr1:59176200-59183200 | Weak transcription | ES-WA7 Cell Line | embryonic stem cell |
| 4 | chr1:59176600-59183800 | Weak transcription | Breast variant Human Mammary Epithelial Cells (vHMEC) | Breast |
| 5 | chr1:59176800-59188800 | Weak transcription | iPS DF 19.11 Cell Line | embryonic stem cell |
| 6 | chr1:59177400-59184000 | Weak transcription | Primary neutrophils fromperipheralblood | blood |
| 7 | chr1:59180600-59192800 | Weak transcription | H1 BMP4 Derived Trophoblast Cultured Cells | ES cell derived |
| 8 | chr1:59181200-59181800 | Enhancers | Fetal Intestine Large | intestine |
