Variant report

Variant rs146230627
Chromosome Location chr1:161414634-161414635
allele C/G
Outlinks Ensembl   UCSC
Chromatin state (count:11 , 50 per page) page: 1
No. Chromosome Location Chromatin state Cell line Tissue
1 chr1:161414600-161414800 Flanking Bivalent TSS/Enh iPS DF 19.11 Cell Line embryonic stem cell
2 chr1:161414600-161414800 Bivalent Enhancer Foreskin Fibroblast Primary Cells skin02 Skin
3 chr1:161414600-161414800 Flanking Bivalent TSS/Enh Skeletal Muscle Female skeletal muscle
4 chr1:161414600-161415000 Bivalent Enhancer H1 Derived Mesenchymal Stem Cells ES cell derived
5 chr1:161414600-161415000 Bivalent/Poised TSS iPS-15b Cell Line embryonic stem cell
6 chr1:161414600-161415000 Bivalent Enhancer iPS DF 6.9 Cell Line embryonic stem cell
7 chr1:161414600-161415000 ZNF genes & repeats Primary neutrophils fromperipheralblood blood
8 chr1:161414600-161415000 Bivalent Enhancer Esophagus oesophagus
9 chr1:161414600-161415000 ZNF genes & repeats Gastric stomach
10 chr1:161414600-161415000 ZNF genes & repeats Pancreas Pancrea
11 chr1:161414600-161415000 ZNF genes & repeats Spleen Spleen

Quick Search:


  
Input of quick search could be:

what's new

Quick links