Variant report
| Variant | rs35787799 |
|---|---|
| Chromosome Location | chr1:222986631-222986632 |
| allele | A/G |
| Outlinks | Ensembl UCSC |
| No. | Chromosome Location | Chromatin state | Cell line | Tissue |
|---|---|---|---|---|
| 1 | chr1:222958800-222987800 | Weak transcription | Foreskin Melanocyte Primary Cells skin01 | Skin |
| 2 | chr1:222983600-222987800 | Enhancers | HepG2 | liver |
| 3 | chr1:222984200-222987200 | Weak transcription | Foreskin Melanocyte Primary Cells skin03 | Skin |
| 4 | chr1:222985400-222987200 | Weak transcription | Fetal Kidney | kidney |
| 5 | chr1:222985600-222986800 | Weak transcription | Fetal Intestine Small | intestine |
| 6 | chr1:222985600-222987000 | Weak transcription | Fetal Intestine Large | intestine |
| 7 | chr1:222986400-222987800 | Weak transcription | iPS DF 19.11 Cell Line | embryonic stem cell |
| 8 | chr1:222986400-222987800 | Enhancers | NHLF | lung |
| 9 | chr1:222986600-222987200 | Enhancers | NH-A | brain |
| 10 | chr1:222986600-222987400 | Enhancers | Foreskin Fibroblast Primary Cells skin02 | Skin |
| 11 | chr1:222986600-222988000 | Enhancers | H1 Derived Mesenchymal Stem Cells | ES cell derived |
