Variant report

Variant rs35061659
Chromosome Location chr8:124985014-124985015
allele A/G
Outlinks Ensembl   UCSC
Chromatin state (count:17 , 50 per page) page: 1
No. Chromosome Location Chromatin state Cell line Tissue
1 chr8:124967200-124987000 Weak transcription Fetal Stomach stomach
2 chr8:124971800-125052000 Weak transcription Gastric stomach
3 chr8:124976800-124989000 Weak transcription Stomach Mucosa stomach
4 chr8:124982800-124985200 Enhancers Skeletal Muscle Male skeletal muscle
5 chr8:124984200-124985600 Enhancers Primary hematopoietic stem cells G-CSF-mobilized Male --
6 chr8:124984200-124994600 Strong transcription Adipose Derived Mesenchymal Stem Cell Cultured Cells ES cell derived
7 chr8:124984600-124985400 Enhancers Primary hematopoietic stem cells blood
8 chr8:124984800-124985200 Enhancers HUES6 Cell Line embryonic stem cell
9 chr8:124984800-124985200 Enhancers HUES64 Cell Line embryonic stem cell
10 chr8:124984800-124985400 Enhancers ES-I3 Cell Line embryonic stem cell
11 chr8:124984800-124985400 Enhancers iPS-20b Cell Line embryonic stem cell
12 chr8:124984800-124985600 Enhancers ES-WA7 Cell Line embryonic stem cell
13 chr8:124984800-124985600 Enhancers Primary B cells from peripheral blood blood
14 chr8:124984800-124985600 Enhancers Primary hematopoietic stem cells short term culture blood
15 chr8:124984800-124985800 Enhancers Primary hematopoietic stem cells G-CSF-mobilized Female --
16 chr8:124985000-124985400 Bivalent Enhancer H9 Derived Neuron Cultured Cells ES cell derived
17 chr8:124985000-124985400 Enhancers iPS-15b Cell Line embryonic stem cell

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