Variant report

Variant rs4979392
Chromosome Location chr9:117204363-117204364
allele A/G
Outlinks Ensembl   UCSC
Chromatin state (count:19 , 50 per page) page: 1
No. Chromosome Location Chromatin state Cell line Tissue
1 chr9:117187000-117213800 Weak transcription Thymus Thymus
2 chr9:117189000-117215200 Weak transcription Fetal Intestine Small intestine
3 chr9:117196600-117208400 Weak transcription Breast variant Human Mammary Epithelial Cells (vHMEC) Breast
4 chr9:117198600-117208400 Weak transcription Foreskin Melanocyte Primary Cells skin01 Skin
5 chr9:117200400-117204400 Weak transcription Foreskin Melanocyte Primary Cells skin03 Skin
6 chr9:117200600-117204800 Weak transcription Pancreas Pancrea
7 chr9:117200600-117208000 Weak transcription Fetal Adrenal Gland Adrenal Gland
8 chr9:117203000-117237800 Weak transcription Placenta Amnion Placenta Amnion
9 chr9:117203200-117204400 Enhancers Brain Anterior Caudate brain
10 chr9:117203200-117206600 Enhancers Brain Inferior Temporal Lobe brain
11 chr9:117203400-117226800 Weak transcription Stomach Smooth Muscle stomach
12 chr9:117204000-117204800 Active TSS Brain Cingulate Gyrus brain
13 chr9:117204000-117205000 Enhancers Fetal Lung lung
14 chr9:117204000-117206400 Enhancers Brain Angular Gyrus brain
15 chr9:117204200-117204600 Flanking Active TSS Brain Hippocampus Middle brain
16 chr9:117204200-117204600 Weak transcription Brain Substantia Nigra brain
17 chr9:117204200-117205000 Enhancers Mesenchymal Stem Cell Derived Adipocyte Cultured Cells ES cell derived
18 chr9:117204200-117205000 Enhancers Ovary ovary
19 chr9:117204200-117212600 Weak transcription Brain Dorsolateral Prefrontal Cortex brain

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