Variant report

Variant rs28463632
Chromosome Location chr9:117198539-117198540
allele C/G
Outlinks Ensembl   UCSC
Chromatin state (count:18 , 50 per page) page: 1
No. Chromosome Location Chromatin state Cell line Tissue
1 chr9:117161200-117199200 Weak transcription Right Atrium heart
2 chr9:117187000-117213800 Weak transcription Thymus Thymus
3 chr9:117189000-117215200 Weak transcription Fetal Intestine Small intestine
4 chr9:117193400-117200600 Enhancers Fetal Adrenal Gland Adrenal Gland
5 chr9:117196600-117208400 Weak transcription Breast variant Human Mammary Epithelial Cells (vHMEC) Breast
6 chr9:117197000-117198600 Enhancers Brain Inferior Temporal Lobe brain
7 chr9:117197400-117198600 Enhancers Foreskin Melanocyte Primary Cells skin01 Skin
8 chr9:117197400-117199800 Weak transcription Pancreas Pancrea
9 chr9:117197600-117199000 Enhancers Foreskin Melanocyte Primary Cells skin03 Skin
10 chr9:117197600-117199800 Weak transcription HepG2 liver
11 chr9:117197600-117202600 Weak transcription Breast Myoepithelial Primary Cells Breast
12 chr9:117197800-117198600 Enhancers Fetal Lung lung
13 chr9:117198000-117201400 Weak transcription Brain Cingulate Gyrus brain
14 chr9:117198000-117204200 Weak transcription Ovary ovary
15 chr9:117198200-117199800 Weak transcription Brain Substantia Nigra brain
16 chr9:117198400-117198600 Enhancers Brain Angular Gyrus brain
17 chr9:117198400-117202800 Weak transcription Brain Hippocampus Middle brain
18 chr9:117198400-117203200 Weak transcription Brain Anterior Caudate brain

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