Variant report

Variant rs192511221
Chromosome Location chr2:180067365-180067366
allele A/G
Outlinks Ensembl   UCSC
Chromatin state (count:12 , 50 per page) page: 1
No. Chromosome Location Chromatin state Cell line Tissue
1 chr2:180032200-180067600 Weak transcription Foreskin Fibroblast Primary Cells skin02 Skin
2 chr2:180065600-180068200 Weak transcription Fetal Stomach stomach
3 chr2:180066800-180067600 ZNF genes & repeats Fetal Kidney kidney
4 chr2:180066800-180067800 ZNF genes & repeats HepG2 liver
5 chr2:180066800-180068400 ZNF genes & repeats Breast variant Human Mammary Epithelial Cells (vHMEC) Breast
6 chr2:180066800-180068800 ZNF genes & repeats iPS-20b Cell Line embryonic stem cell
7 chr2:180067000-180068400 ZNF genes & repeats Primary hematopoietic stem cells blood
8 chr2:180067000-180068600 ZNF genes & repeats Monocytes-CD14+_RO01746 blood
9 chr2:180067000-180069200 ZNF genes & repeats hESC Derived CD184+ Endoderm Cultured Cells ES cell derived
10 chr2:180067200-180068000 ZNF genes & repeats Pancreatic Islets Pancreatic Islet
11 chr2:180067200-180068200 ZNF genes & repeats Fetal Muscle Trunk muscle
12 chr2:180067200-180068800 ZNF genes & repeats Primary hematopoietic stem cells G-CSF-mobilized Male --

Quick Search:


  
Input of quick search could be:

what's new

Quick links