Variant report

Variant rs529168468
Chromosome Location chr9:136861941-136861942
allele C/T
Outlinks Ensembl   UCSC
Chromatin state (count:17 , 50 per page) page: 1
No. Chromosome Location Chromatin state Cell line Tissue
1 chr9:136859600-136864800 Weak transcription Fetal Lung lung
2 chr9:136859600-136875400 Weak transcription Spleen Spleen
3 chr9:136859800-136862000 Weak transcription Pancreas Pancrea
4 chr9:136860000-136862000 Weak transcription H1 BMP4 Derived Trophoblast Cultured Cells ES cell derived
5 chr9:136860000-136864000 Weak transcription Brain Germinal Matrix brain
6 chr9:136860200-136864200 Weak transcription Cortex derived primary cultured neurospheres brain
7 chr9:136860200-136865200 Weak transcription Ganglion Eminence derived primary cultured neurospheres brain
8 chr9:136860400-136862800 Weak transcription ES-UCSF4 Cell Line embryonic stem cell
9 chr9:136860400-136862800 Weak transcription Fetal Brain Male brain
10 chr9:136860400-136864000 Weak transcription Fetal Brain Female brain
11 chr9:136860600-136863400 Weak transcription HSMM muscle
12 chr9:136861000-136864800 Weak transcription H1 Derived Mesenchymal Stem Cells ES cell derived
13 chr9:136861200-136862000 Weak transcription Breast Myoepithelial Primary Cells Breast
14 chr9:136861200-136862400 Enhancers HSMMtube muscle
15 chr9:136861200-136862800 Enhancers Fetal Muscle Leg muscle
16 chr9:136861600-136862200 Bivalent Enhancer Fetal Muscle Trunk muscle
17 chr9:136861800-136862200 ZNF genes & repeats iPS DF 19.11 Cell Line embryonic stem cell

Quick Search:


  
Input of quick search could be:

what's new

Quick links