Variant report

Variant rs10979219
Chromosome Location chr9:110881731-110881732
allele C/T
Outlinks Ensembl   UCSC
Chromatin state (count:10 , 50 per page) page: 1
No. Chromosome Location Chromatin state Cell line Tissue
1 chr9:110868600-110899800 Weak transcription H9 Cell Line embryonic stem cell
2 chr9:110876800-110883800 Weak transcription K562 blood
3 chr9:110878200-110883000 Enhancers Stomach Mucosa stomach
4 chr9:110880200-110881800 Enhancers Esophagus oesophagus
5 chr9:110880400-110882200 Enhancers Foreskin Keratinocyte Primary Cells skin03 Skin
6 chr9:110881600-110882000 Enhancers Breast variant Human Mammary Epithelial Cells (vHMEC) Breast
7 chr9:110881600-110882000 Enhancers Foreskin Keratinocyte Primary Cells skin02 Skin
8 chr9:110881600-110882000 Enhancers HMEC breast
9 chr9:110881600-110882400 Enhancers Pancreas Pancrea
10 chr9:110881600-110883000 Enhancers Gastric stomach

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