Variant report

Variant rs10094884
Chromosome Location chr8:49568947-49568948
allele C/T
Outlinks Ensembl   UCSC
Chromatin state (count:15 , 50 per page) page: 1
No. Chromosome Location Chromatin state Cell line Tissue
1 chr8:49563000-49569400 Weak transcription Spleen Spleen
2 chr8:49563200-49572800 Weak transcription Pancreas Pancrea
3 chr8:49564400-49571200 Weak transcription Breast Myoepithelial Primary Cells Breast
4 chr8:49565000-49570200 Weak transcription Aorta Aorta
5 chr8:49567400-49575800 Weak transcription Foreskin Fibroblast Primary Cells skin01 Skin
6 chr8:49567600-49569000 Weak transcription H1 BMP4 Derived Trophoblast Cultured Cells ES cell derived
7 chr8:49567600-49569200 Weak transcription Fetal Stomach stomach
8 chr8:49567800-49569600 Weak transcription hESC Derived CD56+ Mesoderm Cultured Cells ES cell derived
9 chr8:49568200-49569200 Weak transcription iPS DF 19.11 Cell Line embryonic stem cell
10 chr8:49568400-49569400 Enhancers Mesenchymal Stem Cell Derived Adipocyte Cultured Cells ES cell derived
11 chr8:49568400-49569600 Enhancers Monocytes-CD14+_RO01746 blood
12 chr8:49568400-49569800 Enhancers Primary monocytes fromperipheralblood blood
13 chr8:49568600-49570200 Enhancers Fetal Lung lung
14 chr8:49568800-49569000 Enhancers Primary neutrophils fromperipheralblood blood
15 chr8:49568800-49569200 Enhancers Adipose Derived Mesenchymal Stem Cell Cultured Cells ES cell derived

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