Variant report

Variant rs13247877
Chromosome Location chr7:98798766-98798767
allele C/T
Outlinks Ensembl   UCSC
Chromatin state (count:16 , 50 per page) page: 1
No. Chromosome Location Chromatin state Cell line Tissue
1 chr7:98792200-98803600 Weak transcription Stomach Mucosa stomach
2 chr7:98797800-98800000 Enhancers Placenta Placenta
3 chr7:98798000-98798800 Enhancers Foreskin Fibroblast Primary Cells skin01 Skin
4 chr7:98798000-98799200 Enhancers NHEK skin
5 chr7:98798000-98799600 Enhancers HMEC breast
6 chr7:98798000-98800600 Weak transcription Primary T killer naive cells fromperipheralblood blood
7 chr7:98798200-98799200 Enhancers Bone Marrow Derived Cultured Mesenchymal Stem Cells Bone marrow
8 chr7:98798200-98799200 Enhancers Osteobl bone
9 chr7:98798200-98799400 Enhancers Hela-S3 cervix
10 chr7:98798400-98799200 Enhancers IMR90 fetal lung fibroblasts Cell Line lung
11 chr7:98798400-98799200 Enhancers Adipose Derived Mesenchymal Stem Cell Cultured Cells ES cell derived
12 chr7:98798400-98799200 Enhancers Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells embryonic stem cell
13 chr7:98798400-98799200 Enhancers Foreskin Keratinocyte Primary Cells skin02 Skin
14 chr7:98798600-98799000 Enhancers NH-A brain
15 chr7:98798600-98799200 Enhancers A549 lung
16 chr7:98798600-98800200 Weak transcription Breast variant Human Mammary Epithelial Cells (vHMEC) Breast

Quick Search:


  
Input of quick search could be:

what's new

Quick links