Variant report
| Variant | rs546549828 |
|---|---|
| Chromosome Location | chr7:128705883-128705884 |
| allele | A/T |
| Outlinks | Ensembl UCSC |
| No. | Chromosome Location | Chromatin state | Cell line | Tissue |
|---|---|---|---|---|
| 1 | chr7:128695800-128706200 | Weak transcription | H9 Cell Line | embryonic stem cell |
| 2 | chr7:128696200-128706400 | Weak transcription | Right Atrium | heart |
| 3 | chr7:128696600-128706200 | Weak transcription | Foreskin Melanocyte Primary Cells skin03 | Skin |
| 4 | chr7:128703200-128706800 | Weak transcription | iPS-20b Cell Line | embryonic stem cell |
| 5 | chr7:128704800-128706000 | Enhancers | K562 | blood |
| 6 | chr7:128705200-128708600 | Weak transcription | Monocytes-CD14+_RO01746 | blood |
| 7 | chr7:128705400-128706400 | Weak transcription | iPS DF 19.11 Cell Line | embryonic stem cell |
| 8 | chr7:128705600-128706600 | Weak transcription | Fetal Intestine Small | intestine |
| 9 | chr7:128705600-128706800 | Weak transcription | GM12878-XiMat | blood |
| 10 | chr7:128705800-128706200 | Weak transcription | H1 Derived Mesenchymal Stem Cells | ES cell derived |
| 11 | chr7:128705800-128706200 | Weak transcription | Fetal Intestine Large | intestine |
