Variant report

Variant rs11790176
Chromosome Location chr9:110710983-110710984
allele C/T
Outlinks Ensembl   UCSC
Chromatin state (count:12 , 50 per page) page: 1
No. Chromosome Location Chromatin state Cell line Tissue
1 chr9:110702200-110711000 Weak transcription Fetal Intestine Large intestine
2 chr9:110704000-110714000 Weak transcription Breast variant Human Mammary Epithelial Cells (vHMEC) Breast
3 chr9:110707400-110712600 Enhancers Primary monocytes fromperipheralblood blood
4 chr9:110709800-110712400 Enhancers Foreskin Melanocyte Primary Cells skin03 Skin
5 chr9:110710400-110711000 Enhancers Muscle Satellite Cultured Cells --
6 chr9:110710400-110711000 Enhancers HSMM muscle
7 chr9:110710600-110711000 Enhancers Foreskin Melanocyte Primary Cells skin01 Skin
8 chr9:110710600-110711200 Enhancers Stomach Mucosa stomach
9 chr9:110710600-110711600 Enhancers Mesenchymal Stem Cell Derived Adipocyte Cultured Cells ES cell derived
10 chr9:110710600-110711800 Enhancers Adipose Derived Mesenchymal Stem Cell Cultured Cells ES cell derived
11 chr9:110710600-110712400 Enhancers Monocytes-CD14+_RO01746 blood
12 chr9:110710800-110711200 Weak transcription Gastric stomach

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