Variant report
Variant | rs6675266 |
---|---|
Chromosome Location | chr1:220105116-220105117 |
allele | C/T |
Outlinks | Ensembl   UCSC |
No. | Chromosome Location | Chromatin state | Cell line | Tissue |
---|---|---|---|---|
1 | chr1:220102800-220106200 | Enhancers | Liver | Liver |
2 | chr1:220103400-220105800 | Enhancers | Fetal Intestine Small | intestine |
3 | chr1:220103600-220105600 | Enhancers | Fetal Intestine Large | intestine |
4 | chr1:220104000-220105200 | Enhancers | HepG2 | liver |
5 | chr1:220104800-220108000 | Weak transcription | K562 | blood |