Variant report
| Variant | rs58765710 |
|---|---|
| Chromosome Location | chr5:114673522-114673523 |
| allele | A/T |
| Outlinks | Ensembl UCSC |
| No. | Chromosome Location | Chromatin state | Cell line | Tissue |
|---|---|---|---|---|
| 1 | chr5:114672000-114673600 | Enhancers | Foreskin Melanocyte Primary Cells skin03 | Skin |
| 2 | chr5:114672400-114677200 | Weak transcription | Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells | embryonic stem cell |
| 3 | chr5:114673000-114674600 | Enhancers | Fetal Intestine Small | intestine |
| 4 | chr5:114673000-114678400 | Weak transcription | Cortex derived primary cultured neurospheres | brain |
| 5 | chr5:114673000-114678400 | Weak transcription | Ganglion Eminence derived primary cultured neurospheres | brain |
| 6 | chr5:114673200-114673600 | Enhancers | Mesenchymal Stem Cell Derived Adipocyte Cultured Cells | ES cell derived |
| 7 | chr5:114673200-114673600 | Enhancers | Rectal Mucosa Donor 29 | rectum |
| 8 | chr5:114673200-114673800 | Enhancers | Fetal Intestine Large | intestine |
| 9 | chr5:114673200-114674200 | Enhancers | HepG2 | liver |
| 10 | chr5:114673400-114674200 | Enhancers | Liver | Liver |
