Variant report

Variant rs1339759
Chromosome Location chr9:110711586-110711587
allele C/G
Outlinks Ensembl   UCSC
Chromatin state (count:11 , 50 per page) page: 1
No. Chromosome Location Chromatin state Cell line Tissue
1 chr9:110704000-110714000 Weak transcription Breast variant Human Mammary Epithelial Cells (vHMEC) Breast
2 chr9:110707400-110712600 Enhancers Primary monocytes fromperipheralblood blood
3 chr9:110709800-110712400 Enhancers Foreskin Melanocyte Primary Cells skin03 Skin
4 chr9:110710600-110711600 Enhancers Mesenchymal Stem Cell Derived Adipocyte Cultured Cells ES cell derived
5 chr9:110710600-110711800 Enhancers Adipose Derived Mesenchymal Stem Cell Cultured Cells ES cell derived
6 chr9:110710600-110712400 Enhancers Monocytes-CD14+_RO01746 blood
7 chr9:110711000-110712000 Enhancers Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells embryonic stem cell
8 chr9:110711200-110711600 Weak transcription Fetal Intestine Large intestine
9 chr9:110711200-110711600 Enhancers Gastric stomach
10 chr9:110711200-110715200 Weak transcription Stomach Mucosa stomach
11 chr9:110711400-110712200 Enhancers Primary neutrophils fromperipheralblood blood

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