Variant report

Variant rs28609008
Chromosome Location chr9:139878622-139878623
allele C/T
Outlinks Ensembl   UCSC
Chromatin state (count:17 , 50 per page) page: 1
No. Chromosome Location Chromatin state Cell line Tissue
1 chr9:139873600-139886200 Weak transcription Pancreas Pancrea
2 chr9:139873800-139879600 Weak transcription H9 Cell Line embryonic stem cell
3 chr9:139875600-139879000 Enhancers Brain Hippocampus Middle brain
4 chr9:139876600-139879400 Enhancers Right Ventricle heart
5 chr9:139876800-139879400 Enhancers Brain Dorsolateral Prefrontal Cortex brain
6 chr9:139876800-139880800 Enhancers Brain Substantia Nigra brain
7 chr9:139877000-139879600 Enhancers Brain Anterior Caudate brain
8 chr9:139877000-139879600 Enhancers Brain Inferior Temporal Lobe brain
9 chr9:139877600-139878800 Weak transcription Left Ventricle heart
10 chr9:139877600-139879200 Weak transcription Placenta Placenta
11 chr9:139878000-139879200 Enhancers Brain Cingulate Gyrus brain
12 chr9:139878200-139879800 Enhancers Brain Angular Gyrus brain
13 chr9:139878400-139879400 Bivalent/Poised TSS Foreskin Fibroblast Primary Cells skin02 Skin
14 chr9:139878400-139879800 Enhancers Hela-S3 cervix
15 chr9:139878600-139878800 Bivalent/Poised TSS H1 BMP4 Derived Trophoblast Cultured Cells ES cell derived
16 chr9:139878600-139878800 Bivalent Enhancer HepG2 liver
17 chr9:139878600-139879200 Enhancers iPS DF 19.11 Cell Line embryonic stem cell

Quick Search:


  
Input of quick search could be:

what's new

Quick links