Variant report
Variant | rs16898397 |
---|---|
Chromosome Location | chr5:68334036-68334037 |
allele | A/C |
Outlinks | Ensembl   UCSC |
No. | Chromosome Location | Chromatin state | Cell line | Tissue |
---|---|---|---|---|
1 | chr5:68330600-68339000 | Weak transcription | Breast variant Human Mammary Epithelial Cells (vHMEC) | Breast |
2 | chr5:68332400-68338400 | Weak transcription | Foreskin Keratinocyte Primary Cells skin02 | Skin |
3 | chr5:68332400-68338800 | Weak transcription | NHEK | skin |
4 | chr5:68333000-68338400 | Weak transcription | K562 | blood |
5 | chr5:68334000-68334200 | Bivalent Enhancer | HepG2 | liver |