Variant report

Variant rs2065394
Chromosome Location chr9:104216405-104216406
allele C/G
Outlinks Ensembl   UCSC
Chromatin state (count:15 , 50 per page) page: 1
No. Chromosome Location Chromatin state Cell line Tissue
1 chr9:104212000-104216600 Weak transcription H1 Derived Mesenchymal Stem Cells ES cell derived
2 chr9:104212000-104221200 Weak transcription H9 Cell Line embryonic stem cell
3 chr9:104212000-104241400 Weak transcription iPS DF 6.9 Cell Line embryonic stem cell
4 chr9:104212200-104219000 Weak transcription Liver Liver
5 chr9:104215400-104217400 Enhancers Fetal Adrenal Gland Adrenal Gland
6 chr9:104215600-104216800 Enhancers Fetal Intestine Small intestine
7 chr9:104215800-104216800 Enhancers Fetal Intestine Large intestine
8 chr9:104215800-104217200 Enhancers Adipose Derived Mesenchymal Stem Cell Cultured Cells ES cell derived
9 chr9:104216000-104216800 Enhancers NHDF-Ad bronchial
10 chr9:104216000-104216800 Enhancers Osteobl bone
11 chr9:104216200-104216800 Weak transcription Mesenchymal Stem Cell Derived Adipocyte Cultured Cells ES cell derived
12 chr9:104216200-104217000 Enhancers IMR90 fetal lung fibroblasts Cell Line lung
13 chr9:104216200-104218000 Weak transcription Adipose Nuclei Adipose
14 chr9:104216400-104217800 Weak transcription Bone Marrow Derived Cultured Mesenchymal Stem Cells Bone marrow
15 chr9:104216400-104218200 Weak transcription HepG2 liver

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