Variant report

Variant rs2913826
Chromosome Location chr5:177717640-177717641
allele C/T
Outlinks Ensembl   UCSC
Chromatin state (count:10 , 50 per page) page: 1
No. Chromosome Location Chromatin state Cell line Tissue
1 chr5:177703600-177728800 Weak transcription Right Atrium heart
2 chr5:177713400-177719000 Enhancers Breast Myoepithelial Primary Cells Breast
3 chr5:177715200-177718600 Enhancers Cortex derived primary cultured neurospheres brain
4 chr5:177716600-177720200 Weak transcription H1 Derived Neuronal Progenitor Cultured Cells ES cell derived
5 chr5:177716800-177717800 Weak transcription Fetal Lung lung
6 chr5:177717400-177717800 Bivalent Enhancer Skeletal Muscle Female skeletal muscle
7 chr5:177717400-177717800 Enhancers K562 blood
8 chr5:177717400-177718200 Bivalent Enhancer Esophagus oesophagus
9 chr5:177717400-177718400 ZNF genes & repeats iPS DF 19.11 Cell Line embryonic stem cell
10 chr5:177717600-177718600 Bivalent Enhancer Fetal Stomach stomach

Quick Search:


  
Input of quick search could be:

what's new

Quick links