Variant report

Variant rs10889864
Chromosome Location chr1:70469075-70469076
allele G/T
Outlinks Ensembl   UCSC
Chromatin state (count:12 , 50 per page) page: 1
No. Chromosome Location Chromatin state Cell line Tissue
1 chr1:70450800-70481200 Weak transcription Fetal Brain Female brain
2 chr1:70464800-70509000 Weak transcription Brain Angular Gyrus brain
3 chr1:70468000-70469200 Weak transcription Fetal Lung lung
4 chr1:70468600-70469600 Enhancers Foreskin Keratinocyte Primary Cells skin02 Skin
5 chr1:70468600-70470000 Enhancers Primary monocytes fromperipheralblood blood
6 chr1:70468800-70469600 Enhancers Foreskin Melanocyte Primary Cells skin03 Skin
7 chr1:70468800-70469600 Enhancers NHEK skin
8 chr1:70468800-70469800 Enhancers Muscle Satellite Cultured Cells --
9 chr1:70469000-70469400 Enhancers Primary hematopoietic stem cells short term culture blood
10 chr1:70469000-70469600 Enhancers Adipose Derived Mesenchymal Stem Cell Cultured Cells ES cell derived
11 chr1:70469000-70469800 Enhancers HUVEC blood vessel
12 chr1:70469000-70470400 Enhancers Foreskin Keratinocyte Primary Cells skin03 Skin

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