Variant report
| Variant | rs34849016 |
|---|---|
| Chromosome Location | chr7:117111801-117111802 |
| allele | G/T |
| Outlinks | Ensembl UCSC |
| No. | Chromosome Location | Chromatin state | Cell line | Tissue |
|---|---|---|---|---|
| 1 | chr7:117110400-117113200 | Enhancers | Dnd41 | blood |
| 2 | chr7:117110600-117113400 | Enhancers | Fetal Heart | heart |
| 3 | chr7:117111200-117112000 | Weak transcription | Small Intestine | intestine |
| 4 | chr7:117111200-117112600 | Weak transcription | Brain Substantia Nigra | brain |
| 5 | chr7:117111200-117112600 | Enhancers | GM12878-XiMat | blood |
| 6 | chr7:117111200-117113600 | Weak transcription | Pancreas | Pancrea |
| 7 | chr7:117111800-117112000 | Enhancers | Brain Hippocampus Middle | brain |
