Variant report
| Variant | rs6690929 |
|---|---|
| Chromosome Location | chr1:168723582-168723583 |
| allele | A/G |
| Outlinks | Ensembl UCSC |
| No. | Chromosome Location | Chromatin state | Cell line | Tissue |
|---|---|---|---|---|
| 1 | chr1:168711200-168724200 | Weak transcription | H1 BMP4 Derived Trophoblast Cultured Cells | ES cell derived |
| 2 | chr1:168720800-168724000 | Weak transcription | Fetal Heart | heart |
| 3 | chr1:168721000-168723600 | Weak transcription | Fetal Kidney | kidney |
| 4 | chr1:168721000-168723800 | Weak transcription | Placenta Amnion | Placenta Amnion |
| 5 | chr1:168721200-168725400 | Weak transcription | Pancreatic Islets | Pancreatic Islet |
| 6 | chr1:168721400-168725200 | Weak transcription | hESC Derived CD184+ Endoderm Cultured Cells | ES cell derived |
| 7 | chr1:168722000-168728200 | Weak transcription | Pancreas | Pancrea |
| 8 | chr1:168722200-168724200 | Weak transcription | H1 Derived Mesenchymal Stem Cells | ES cell derived |
| 9 | chr1:168722200-168727400 | Weak transcription | Fetal Intestine Small | intestine |
| 10 | chr1:168723400-168724000 | Enhancers | HepG2 | liver |
