Variant report

Variant rs1191805
Chromosome Location chr2:20220339-20220340
allele C/T
Outlinks Ensembl   UCSC
Chromatin state (count:16 , 50 per page) page: 1
No. Chromosome Location Chromatin state Cell line Tissue
1 chr2:20213000-20220600 Weak transcription Foreskin Fibroblast Primary Cells skin02 Skin
2 chr2:20213000-20227200 Weak transcription Ovary ovary
3 chr2:20213200-20225000 Weak transcription Muscle Satellite Cultured Cells --
4 chr2:20213200-20227000 Weak transcription Bone Marrow Derived Cultured Mesenchymal Stem Cells Bone marrow
5 chr2:20213200-20227000 Weak transcription Aorta Aorta
6 chr2:20213400-20227400 Weak transcription Fetal Kidney kidney
7 chr2:20213400-20232200 Weak transcription Right Ventricle heart
8 chr2:20213600-20227000 Weak transcription Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells embryonic stem cell
9 chr2:20216400-20227800 Weak transcription Fetal Intestine Large intestine
10 chr2:20216400-20228800 Weak transcription Pancreatic Islets Pancreatic Islet
11 chr2:20216600-20220400 Weak transcription HepG2 liver
12 chr2:20216800-20224800 Weak transcription Breast variant Human Mammary Epithelial Cells (vHMEC) Breast
13 chr2:20217400-20220400 Weak transcription H1 Derived Mesenchymal Stem Cells ES cell derived
14 chr2:20219400-20227000 Weak transcription Left Ventricle heart
15 chr2:20220000-20221200 Weak transcription Stomach Smooth Muscle stomach
16 chr2:20220200-20222400 ZNF genes & repeats hESC Derived CD184+ Endoderm Cultured Cells ES cell derived

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