Variant report

Variant rs10756860
Chromosome Location chr9:17309336-17309337
allele C/T
Outlinks Ensembl   UCSC
Chromatin state (count:17 , 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 chr9:17284400-17309600 Weak transcription Ovary ovary
4 chr9:17284400-17344800 Weak transcription Primary hematopoietic stem cells blood
5 chr9:17285000-17311600 Weak transcription Breast Myoepithelial Primary Cells Breast
6 chr9:17292200-17367200 Weak transcription H1 Derived Mesenchymal Stem Cells ES cell derived
7 chr9:17293800-17314200 Weak transcription Foreskin Melanocyte Primary Cells skin03 Skin
8 chr9:17294000-17317600 Weak transcription Liver Liver
9 chr9:17294000-17334000 Weak transcription Fetal Stomach stomach
10 chr9:17294000-17346000 Weak transcription Fetal Muscle Leg muscle
11 chr9:17294600-17311000 Weak transcription Primary monocytes fromperipheralblood blood
12 chr9:17299400-17312000 Weak transcription A549 lung
13 chr9:17300800-17318600 Weak transcription Adipose Derived Mesenchymal Stem Cell Cultured Cells ES cell derived
14 chr9:17301200-17332200 Weak transcription Monocytes-CD14+_RO01746 blood
15 chr9:17307400-17313000 Weak transcription Primary hematopoietic stem cells G-CSF-mobilized Male --
16 chr9:17308600-17322600 Weak transcription Fetal Lung lung
17 chr9:17309200-17312400 Weak transcription Primary neutrophils fromperipheralblood blood

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