Variant report

Variant rs10981789
Chromosome Location chr9:116222054-116222055
allele C/T
Outlinks Ensembl   UCSC
Chromatin state (count:20 , 50 per page) page: 1
No. Chromosome Location Chromatin state Cell line Tissue
1 chr9:116216000-116225400 Weak transcription Gastric stomach
2 chr9:116217400-116225200 Weak transcription Right Ventricle heart
3 chr9:116217600-116225200 Weak transcription H1 Derived Mesenchymal Stem Cells ES cell derived
4 chr9:116218200-116225400 Weak transcription Ganglion Eminence derived primary cultured neurospheres brain
5 chr9:116218600-116229200 Strong transcription Primary hematopoietic stem cells G-CSF-mobilized Male --
6 chr9:116218800-116224200 Weak transcription Skeletal Muscle Female skeletal muscle
7 chr9:116218800-116224800 Weak transcription Brain Hippocampus Middle brain
8 chr9:116218800-116225200 Weak transcription Fetal Intestine Small intestine
9 chr9:116218800-116225200 Weak transcription Small Intestine intestine
10 chr9:116218800-116225400 Weak transcription Pancreas Pancrea
11 chr9:116218800-116225400 Weak transcription Right Atrium heart
12 chr9:116218800-116226000 Weak transcription Fetal Kidney kidney
13 chr9:116219000-116225400 Weak transcription Fetal Intestine Large intestine
14 chr9:116219400-116240000 Strong transcription Primary hematopoietic stem cells G-CSF-mobilized Female --
15 chr9:116219600-116223600 Weak transcription Primary hematopoietic stem cells short term culture blood
16 chr9:116219600-116225400 Weak transcription Aorta Aorta
17 chr9:116219800-116223600 Weak transcription HepG2 liver
18 chr9:116219800-116225000 Weak transcription Placenta Placenta
19 chr9:116220000-116223200 Weak transcription Fetal Heart heart
20 chr9:116220200-116223400 Weak transcription Primary hematopoietic stem cells blood

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