Variant report

Variant rs7853516
Chromosome Location chr9:117203632-117203633
allele C/T
Outlinks Ensembl   UCSC
Chromatin state (count:17 , 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 chr9:117198000-117204200 Weak transcription Ovary ovary
5 chr9:117198600-117204000 Weak transcription Fetal Lung lung
6 chr9:117198600-117208400 Weak transcription Foreskin Melanocyte Primary Cells skin01 Skin
7 chr9:117200400-117204400 Weak transcription Foreskin Melanocyte Primary Cells skin03 Skin
8 chr9:117200600-117204800 Weak transcription Pancreas Pancrea
9 chr9:117200600-117208000 Weak transcription Fetal Adrenal Gland Adrenal Gland
10 chr9:117202600-117204200 Enhancers Brain Substantia Nigra brain
11 chr9:117202800-117204200 Enhancers Brain Hippocampus Middle brain
12 chr9:117203000-117237800 Weak transcription Placenta Amnion Placenta Amnion
13 chr9:117203200-117203800 Enhancers Brain Cingulate Gyrus brain
14 chr9:117203200-117204400 Enhancers Brain Anterior Caudate brain
15 chr9:117203200-117206600 Enhancers Brain Inferior Temporal Lobe brain
16 chr9:117203400-117226800 Weak transcription Stomach Smooth Muscle stomach
17 chr9:117203600-117204000 Weak transcription Brain Angular Gyrus brain

Quick Search:


  
Input of quick search could be:

what's new

Quick links