Variant report

Variant rs10982221
Chromosome Location chr9:117205568-117205569
allele C/T
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 chr9:117200600-117208000 Weak transcription Fetal Adrenal Gland Adrenal Gland
6 chr9:117203000-117237800 Weak transcription Placenta Amnion Placenta Amnion
7 chr9:117203200-117206600 Enhancers Brain Inferior Temporal Lobe brain
8 chr9:117203400-117226800 Weak transcription Stomach Smooth Muscle stomach
9 chr9:117204000-117206400 Enhancers Brain Angular Gyrus brain
10 chr9:117204200-117212600 Weak transcription Brain Dorsolateral Prefrontal Cortex brain
11 chr9:117204600-117206400 Enhancers Brain Substantia Nigra brain
12 chr9:117204800-117206600 Enhancers Brain Cingulate Gyrus brain
13 chr9:117204800-117208400 Weak transcription Foreskin Melanocyte Primary Cells skin03 Skin
14 chr9:117205000-117205800 Enhancers Brain Anterior Caudate brain
15 chr9:117205000-117207800 Weak transcription Mesenchymal Stem Cell Derived Adipocyte Cultured Cells ES cell derived
16 chr9:117205000-117209000 Weak transcription Ovary ovary
17 chr9:117205000-117212400 Weak transcription iPS DF 6.9 Cell Line embryonic stem cell
18 chr9:117205200-117206400 Enhancers Brain Hippocampus Middle brain
19 chr9:117205400-117210800 Weak transcription H1 Derived Mesenchymal Stem Cells ES cell derived

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