Variant report

Variant rs429819
Chromosome Location chr9:93851952-93851953
allele C/G
Outlinks Ensembl   UCSC
Chromatin state (count:12 , 50 per page) page: 1
No. Chromosome Location Chromatin state Cell line Tissue
1 chr9:93847800-93855600 Weak transcription iPS DF 19.11 Cell Line embryonic stem cell
2 chr9:93848200-93852200 Weak transcription Primary hematopoietic stem cells G-CSF-mobilized Female --
3 chr9:93849800-93852000 Weak transcription Foreskin Fibroblast Primary Cells skin01 Skin
4 chr9:93849800-93852200 Weak transcription Skeletal Muscle Female skeletal muscle
5 chr9:93850000-93852000 Weak transcription Fetal Intestine Small intestine
6 chr9:93851600-93852400 Weak transcription H1 Derived Mesenchymal Stem Cells ES cell derived
7 chr9:93851600-93853200 Enhancers HepG2 liver
8 chr9:93851800-93852600 Enhancers Primary Natural Killer cells fromperipheralblood blood
9 chr9:93851800-93852600 Enhancers Foreskin Fibroblast Primary Cells skin02 Skin
10 chr9:93851800-93852600 Enhancers Fetal Heart heart
11 chr9:93851800-93853000 Enhancers Adipose Derived Mesenchymal Stem Cell Cultured Cells ES cell derived
12 chr9:93851800-93853200 Enhancers IMR90 fetal lung fibroblasts Cell Line lung

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