Variant report

Variant rs9995589
Chromosome Location chr4:160427421-160427422
allele C/T
Outlinks Ensembl   UCSC
Chromatin state (count:14 , 50 per page) page: 1
No. Chromosome Location Chromatin state Cell line Tissue
1 chr4:160414400-160430400 Weak transcription Foreskin Keratinocyte Primary Cells skin03 Skin
2 chr4:160424800-160427600 Enhancers Fetal Brain Male brain
3 chr4:160424800-160427800 Enhancers iPS-18 Cell Line embryonic stem cell
4 chr4:160425000-160428000 Enhancers ES-I3 Cell Line embryonic stem cell
5 chr4:160425600-160427600 Enhancers Fetal Adrenal Gland Adrenal Gland
6 chr4:160426000-160430400 Weak transcription H1 Derived Neuronal Progenitor Cultured Cells ES cell derived
7 chr4:160426200-160427600 Enhancers Brain Germinal Matrix brain
8 chr4:160426200-160428400 Weak transcription H1 Derived Mesenchymal Stem Cells ES cell derived
9 chr4:160426800-160427600 Enhancers HSMM muscle
10 chr4:160427000-160427600 Enhancers Bone Marrow Derived Cultured Mesenchymal Stem Cells Bone marrow
11 chr4:160427000-160430400 Weak transcription Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells embryonic stem cell
12 chr4:160427200-160430200 Weak transcription NH-A brain
13 chr4:160427400-160429800 Weak transcription Muscle Satellite Cultured Cells --
14 chr4:160427400-160430200 Weak transcription Liver Liver

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