Variant report
| Variant | rs11572466 |
|---|---|
| Chromosome Location | chr1:217126903-217126904 |
| allele | A/C/G/T |
| Outlinks | Ensembl UCSC |
| No. | Chromosome Location | Chromatin state | Cell line | Tissue |
|---|---|---|---|---|
| 1 | chr1:217122400-217146200 | Weak transcription | Pancreas | Pancrea |
| 2 | chr1:217125200-217135400 | Weak transcription | Fetal Heart | heart |
| 3 | chr1:217125400-217127000 | Enhancers | HUES48 Cell Line | embryonic stem cell |
| 4 | chr1:217125600-217127000 | Enhancers | iPS-15b Cell Line | embryonic stem cell |
| 5 | chr1:217126000-217127000 | Enhancers | HUES64 Cell Line | embryonic stem cell |
| 6 | chr1:217126200-217127000 | Enhancers | iPS DF 19.11 Cell Line | embryonic stem cell |
| 7 | chr1:217126800-217127000 | Enhancers | Left Ventricle | heart |
