Variant report

Variant rs10981936
Chromosome Location chr9:116569775-116569776
allele A/G
Outlinks Ensembl   UCSC
Chromatin state (count:13 , 50 per page) page: 1
No. Chromosome Location Chromatin state Cell line Tissue
1 chr9:116557800-116569800 Weak transcription iPS DF 19.11 Cell Line embryonic stem cell
2 chr9:116567000-116569800 Weak transcription Primary hematopoietic stem cells G-CSF-mobilized Female --
3 chr9:116569400-116569800 Enhancers Ovary ovary
4 chr9:116569600-116569800 Enhancers HUES6 Cell Line embryonic stem cell
5 chr9:116569600-116569800 Enhancers Adipose Nuclei Adipose
6 chr9:116569600-116569800 Flanking Active TSS Colon Smooth Muscle Colon
7 chr9:116569600-116569800 Enhancers Fetal Adrenal Gland Adrenal Gland
8 chr9:116569600-116569800 Enhancers Rectal Mucosa Donor 31 rectum
9 chr9:116569600-116569800 Enhancers Monocytes-CD14+_RO01746 blood
10 chr9:116569600-116570000 Active TSS Primary hematopoietic stem cells G-CSF-mobilized Male --
11 chr9:116569600-116570000 Active TSS Brain Hippocampus Middle brain
12 chr9:116569600-116570000 Active TSS Fetal Kidney kidney
13 chr9:116569600-116570400 Enhancers Liver Liver

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