Variant report

Variant rs16920140
Chromosome Location chr9:104077900-104077901
allele C/T
Outlinks Ensembl   UCSC
Chromatin state (count:21 , 50 per page) page: 1
No. Chromosome Location Chromatin state Cell line Tissue
1 chr9:104073000-104088600 Weak transcription Brain Cingulate Gyrus brain
2 chr9:104073800-104082600 Weak transcription Brain Anterior Caudate brain
3 chr9:104074200-104080800 Enhancers Liver Liver
4 chr9:104074400-104081200 Weak transcription Brain Substantia Nigra brain
5 chr9:104075400-104079600 Weak transcription Fetal Brain Female brain
6 chr9:104075600-104079400 Weak transcription Breast Myoepithelial Primary Cells Breast
7 chr9:104075600-104079800 Weak transcription Fetal Brain Male brain
8 chr9:104075600-104081800 Weak transcription Brain Inferior Temporal Lobe brain
9 chr9:104075600-104088600 Weak transcription Brain Germinal Matrix brain
10 chr9:104075800-104079600 Weak transcription Brain Hippocampus Middle brain
11 chr9:104077200-104079000 Enhancers A549 lung
12 chr9:104077600-104078000 Enhancers HSMMtube muscle
13 chr9:104077600-104078200 Enhancers Fetal Muscle Leg muscle
14 chr9:104077600-104078400 Enhancers Fetal Lung lung
15 chr9:104077600-104078400 Flanking Active TSS HepG2 liver
16 chr9:104077800-104078200 Bivalent Enhancer Primary hematopoietic stem cells short term culture blood
17 chr9:104077800-104078200 Enhancers Left Ventricle heart
18 chr9:104077800-104078200 Enhancers Stomach Mucosa stomach
19 chr9:104077800-104078200 Enhancers Spleen Spleen
20 chr9:104077800-104078400 Bivalent Enhancer Primary hematopoietic stem cells G-CSF-mobilized Male --
21 chr9:104077800-104078600 Enhancers Gastric stomach

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