Variant report

Variant rs1940768
Chromosome Location chr11:106023422-106023423
allele C/T
Outlinks Ensembl   UCSC
Chromatin state (count:15 , 50 per page) page: 1
No. Chromosome Location Chromatin state Cell line Tissue
1 chr11:106022600-106023800 Enhancers Bone Marrow Derived Cultured Mesenchymal Stem Cells Bone marrow
2 chr11:106022600-106023800 Enhancers NH-A brain
3 chr11:106022600-106024000 Enhancers NHEK skin
4 chr11:106022800-106023600 Enhancers Mesenchymal Stem Cell Derived Adipocyte Cultured Cells ES cell derived
5 chr11:106022800-106024000 Enhancers Adipose Derived Mesenchymal Stem Cell Cultured Cells ES cell derived
6 chr11:106022800-106024000 Enhancers Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells embryonic stem cell
7 chr11:106022800-106024200 Enhancers Foreskin Keratinocyte Primary Cells skin02 Skin
8 chr11:106022800-106024200 Enhancers Foreskin Keratinocyte Primary Cells skin03 Skin
9 chr11:106022800-106025200 Enhancers Foreskin Melanocyte Primary Cells skin03 Skin
10 chr11:106023000-106024600 Enhancers Breast variant Human Mammary Epithelial Cells (vHMEC) Breast
11 chr11:106023000-106024800 Enhancers Breast Myoepithelial Primary Cells Breast
12 chr11:106023200-106024200 Weak transcription Foreskin Melanocyte Primary Cells skin01 Skin
13 chr11:106023200-106025000 Enhancers HMEC breast
14 chr11:106023200-106031000 Weak transcription Osteobl bone
15 chr11:106023200-106031200 Weak transcription IMR90 fetal lung fibroblasts Cell Line lung

Quick Search:


  
Input of quick search could be:

what's new

Quick links