Variant report

Variant rs8131832
Chromosome Location chr21:46446618-46446619
allele A/G
Outlinks Ensembl   UCSC
Chromatin state (count:14 , 50 per page) page: 1
No. Chromosome Location Chromatin state Cell line Tissue
1 chr21:46438600-46453000 Weak transcription Placenta Amnion Placenta Amnion
2 chr21:46439400-46452200 Weak transcription Esophagus oesophagus
3 chr21:46440600-46449200 Weak transcription Right Atrium heart
4 chr21:46441600-46449400 Weak transcription Skeletal Muscle Male skeletal muscle
5 chr21:46442200-46450800 Weak transcription Spleen Spleen
6 chr21:46446000-46446800 Enhancers Fetal Muscle Leg muscle
7 chr21:46446000-46447200 Enhancers Fetal Muscle Trunk muscle
8 chr21:46446000-46447600 Enhancers H1 Derived Mesenchymal Stem Cells ES cell derived
9 chr21:46446400-46446800 Enhancers Aorta Aorta
10 chr21:46446600-46447200 Enhancers HUES6 Cell Line embryonic stem cell
11 chr21:46446600-46447200 Genic enhancers iPS DF 6.9 Cell Line embryonic stem cell
12 chr21:46446600-46447600 Enhancers iPS DF 19.11 Cell Line embryonic stem cell
13 chr21:46446600-46447600 Bivalent/Poised TSS Foreskin Fibroblast Primary Cells skin02 Skin
14 chr21:46446600-46451400 Weak transcription Ovary ovary

Quick Search:


  
Input of quick search could be:

what's new

Quick links