Variant report

Variant rs10896812
Chromosome Location chr11:58426000-58426001
allele A/G
Outlinks Ensembl   UCSC
Chromatin state (count:15 , 50 per page) page: 1
No. Chromosome Location Chromatin state Cell line Tissue
1 chr11:58422000-58426200 Weak transcription Fetal Intestine Small intestine
2 chr11:58422200-58426000 Weak transcription NHEK skin
3 chr11:58422400-58426000 Weak transcription Breast variant Human Mammary Epithelial Cells (vHMEC) Breast
4 chr11:58422400-58426000 Weak transcription Fetal Intestine Large intestine
5 chr11:58423400-58427000 Weak transcription H1 BMP4 Derived Trophoblast Cultured Cells ES cell derived
6 chr11:58425600-58428000 Enhancers HMEC breast
7 chr11:58425800-58426200 Enhancers Esophagus oesophagus
8 chr11:58425800-58428000 Enhancers Foreskin Keratinocyte Primary Cells skin02 Skin
9 chr11:58426000-58426400 Enhancers Adipose Derived Mesenchymal Stem Cell Cultured Cells ES cell derived
10 chr11:58426000-58426400 Enhancers Breast Myoepithelial Primary Cells Breast
11 chr11:58426000-58427600 Enhancers Foreskin Keratinocyte Primary Cells skin03 Skin
12 chr11:58426000-58427600 Enhancers NHEK skin
13 chr11:58426000-58427800 Enhancers Breast variant Human Mammary Epithelial Cells (vHMEC) Breast
14 chr11:58426000-58428200 Enhancers Stomach Mucosa stomach
15 chr11:58426000-58429000 Enhancers Fetal Intestine Large intestine

Quick Search:


  
Input of quick search could be:

what's new

Quick links