Variant report
| Variant | rs375182614 |
|---|---|
| Chromosome Location | chr7:128705288-128705289 |
| allele | C/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 | chr7:128703800-128705800 | Enhancers | H1 Derived Mesenchymal Stem Cells | ES cell derived |
| 6 | chr7:128704600-128705800 | Enhancers | Fetal Intestine Large | intestine |
| 7 | chr7:128704800-128705600 | Enhancers | GM12878-XiMat | blood |
| 8 | chr7:128704800-128706000 | Enhancers | K562 | blood |
| 9 | chr7:128705200-128705400 | Enhancers | iPS DF 19.11 Cell Line | embryonic stem cell |
| 10 | chr7:128705200-128705600 | Enhancers | Fetal Intestine Small | intestine |
| 11 | chr7:128705200-128708600 | Weak transcription | Monocytes-CD14+_RO01746 | blood |
