Variant report

Variant rs1358705
Chromosome Location chr12:44287850-44287851
allele C/T
Outlinks Ensembl   UCSC
Chromatin state (count:19 , 50 per page) page: 1
No. Chromosome Location Chromatin state Cell line Tissue
1 chr12:44240400-44293000 Weak transcription Aorta Aorta
2 chr12:44279200-44292600 Weak transcription Left Ventricle heart
3 chr12:44279200-44297600 Weak transcription Foreskin Melanocyte Primary Cells skin01 Skin
4 chr12:44282800-44289800 Weak transcription Sigmoid Colon Sigmoid Colon
5 chr12:44286200-44289200 Weak transcription Foreskin Melanocyte Primary Cells skin03 Skin
6 chr12:44286600-44289000 Weak transcription Fetal Intestine Large intestine
7 chr12:44287000-44290000 Weak transcription HSMMtube muscle
8 chr12:44287400-44288000 Enhancers Foreskin Fibroblast Primary Cells skin01 Skin
9 chr12:44287400-44288000 Enhancers Hela-S3 cervix
10 chr12:44287400-44288000 Enhancers Osteobl bone
11 chr12:44287400-44288200 Enhancers Adipose Derived Mesenchymal Stem Cell Cultured Cells ES cell derived
12 chr12:44287600-44288000 Enhancers IMR90 fetal lung fibroblasts Cell Line lung
13 chr12:44287600-44288000 Enhancers Breast variant Human Mammary Epithelial Cells (vHMEC) Breast
14 chr12:44287600-44288000 Enhancers Muscle Satellite Cultured Cells --
15 chr12:44287600-44288000 Enhancers Psoas Muscle Psoas
16 chr12:44287600-44288000 Enhancers HMEC breast
17 chr12:44287800-44288000 Weak transcription Foreskin Keratinocyte Primary Cells skin03 Skin
18 chr12:44287800-44288000 Enhancers Pancreas Pancrea
19 chr12:44287800-44288000 ZNF genes & repeats Stomach Smooth Muscle stomach

Quick Search:


  
Input of quick search could be:

what's new

Quick links