Variant report

Variant rs4743860
Chromosome Location chr9:92876730-92876731
allele C/T
Outlinks Ensembl   UCSC
Chromatin state (count:10 , 50 per page) page: 1
No. Chromosome Location Chromatin state Cell line Tissue
1 chr9:92874600-92877800 Enhancers Breast variant Human Mammary Epithelial Cells (vHMEC) Breast
2 chr9:92874600-92877800 Enhancers NHDF-Ad bronchial
3 chr9:92875000-92877000 Enhancers Foreskin Keratinocyte Primary Cells skin02 Skin
4 chr9:92875000-92877600 Enhancers NHEK skin
5 chr9:92875000-92878000 Enhancers Foreskin Keratinocyte Primary Cells skin03 Skin
6 chr9:92875800-92876800 Weak transcription Adipose Derived Mesenchymal Stem Cell Cultured Cells ES cell derived
7 chr9:92876200-92877200 Weak transcription Fetal Brain Male brain
8 chr9:92876400-92876800 Enhancers Fetal Brain Female brain
9 chr9:92876400-92877800 Enhancers HMEC breast
10 chr9:92876600-92876800 Enhancers Esophagus oesophagus

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