Variant report

Variant rs16866857
Chromosome Location chr2:180479461-180479462
allele C/G
Outlinks Ensembl   UCSC
Chromatin state (count:17 , 50 per page) page: 1
No. Chromosome Location Chromatin state Cell line Tissue
1 chr2:180476600-180479600 Enhancers Mesenchymal Stem Cell Derived Adipocyte Cultured Cells ES cell derived
2 chr2:180476600-180479600 Enhancers Osteobl bone
3 chr2:180477200-180479800 Enhancers IMR90 fetal lung fibroblasts Cell Line lung
4 chr2:180477200-180480000 Enhancers Placenta Amnion Placenta Amnion
5 chr2:180477200-180480000 Enhancers NHLF lung
6 chr2:180477400-180488200 Weak transcription Pancreas Pancrea
7 chr2:180477800-180484200 Weak transcription hESC Derived CD184+ Endoderm Cultured Cells ES cell derived
8 chr2:180478000-180483000 Weak transcription Skeletal Muscle Male skeletal muscle
9 chr2:180478200-180479600 Enhancers HSMM muscle
10 chr2:180478800-180479600 Enhancers Fetal Lung lung
11 chr2:180478800-180479800 Enhancers HSMMtube muscle
12 chr2:180478800-180481200 Weak transcription H1 Derived Mesenchymal Stem Cells ES cell derived
13 chr2:180478800-180488200 Weak transcription Lung lung
14 chr2:180479000-180479600 Enhancers Foreskin Keratinocyte Primary Cells skin02 Skin
15 chr2:180479000-180479600 Enhancers Foreskin Keratinocyte Primary Cells skin03 Skin
16 chr2:180479000-180487400 Weak transcription Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells embryonic stem cell
17 chr2:180479200-180480000 Enhancers NHEK skin

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