Variant report

Variant rs10756864
Chromosome Location chr9:17314770-17314771
allele A/G
Outlinks Ensembl   UCSC
Chromatin state (count:14 , 50 per page) page: 1
No. Chromosome Location Chromatin state Cell line Tissue
1 chr9:17262800-17339800 Weak transcription Left Ventricle heart
2 chr9:17274800-17323200 Weak transcription Aorta Aorta
3 chr9:17284400-17344800 Weak transcription Primary hematopoietic stem cells blood
4 chr9:17292200-17367200 Weak transcription H1 Derived Mesenchymal Stem Cells ES cell derived
5 chr9:17294000-17317600 Weak transcription Liver Liver
6 chr9:17294000-17334000 Weak transcription Fetal Stomach stomach
7 chr9:17294000-17346000 Weak transcription Fetal Muscle Leg muscle
8 chr9:17300800-17318600 Weak transcription Adipose Derived Mesenchymal Stem Cell Cultured Cells ES cell derived
9 chr9:17301200-17332200 Weak transcription Monocytes-CD14+_RO01746 blood
10 chr9:17308600-17322600 Weak transcription Fetal Lung lung
11 chr9:17311800-17318200 Weak transcription Primary monocytes fromperipheralblood blood
12 chr9:17313400-17333200 Weak transcription Primary hematopoietic stem cells G-CSF-mobilized Male --
13 chr9:17314600-17314800 ZNF genes & repeats Foreskin Melanocyte Primary Cells skin03 Skin
14 chr9:17314600-17315400 Enhancers HSMM muscle

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