Variant report

Variant rs16938569
Chromosome Location chr8:49605990-49605991
allele C/T
Outlinks Ensembl   UCSC
Chromatin state (count:13 , 50 per page) page: 1
No. Chromosome Location Chromatin state Cell line Tissue
1 chr8:49595800-49607600 Weak transcription H1 BMP4 Derived Trophoblast Cultured Cells ES cell derived
2 chr8:49595800-49616800 Weak transcription H1 Derived Mesenchymal Stem Cells ES cell derived
3 chr8:49600800-49607600 Weak transcription Lung lung
4 chr8:49603200-49608800 Weak transcription iPS DF 19.11 Cell Line embryonic stem cell
5 chr8:49604200-49611400 Weak transcription Fetal Brain Female brain
6 chr8:49604600-49608600 Weak transcription Muscle Satellite Cultured Cells --
7 chr8:49604800-49608200 Weak transcription HSMM muscle
8 chr8:49605600-49607200 Enhancers Foreskin Keratinocyte Primary Cells skin02 Skin
9 chr8:49605600-49612000 Enhancers NHEK skin
10 chr8:49605600-49621000 Enhancers Breast Myoepithelial Primary Cells Breast
11 chr8:49605600-49621800 Enhancers Breast variant Human Mammary Epithelial Cells (vHMEC) Breast
12 chr8:49605800-49611800 Enhancers Foreskin Keratinocyte Primary Cells skin03 Skin
13 chr8:49605800-49621200 Enhancers HMEC breast

Quick Search:


  
Input of quick search could be:

what's new

Quick links