Variant report

Variant rs8133212
Chromosome Location chr21:46822612-46822613
allele C/T
Outlinks Ensembl   UCSC
Chromatin state (count:15 , 50 per page) page: 1
No. Chromosome Location Chromatin state Cell line Tissue
1 chr21:46807800-46824400 Weak transcription Right Atrium heart
2 chr21:46822000-46823800 Bivalent Enhancer iPS DF 19.11 Cell Line embryonic stem cell
3 chr21:46822200-46822800 Enhancers Ovary ovary
4 chr21:46822200-46823200 Enhancers Foreskin Keratinocyte Primary Cells skin02 Skin
5 chr21:46822200-46824000 Enhancers Breast Myoepithelial Primary Cells Breast
6 chr21:46822200-46824200 Enhancers iPS DF 6.9 Cell Line embryonic stem cell
7 chr21:46822200-46824400 Enhancers H1 Derived Mesenchymal Stem Cells ES cell derived
8 chr21:46822400-46824200 Enhancers HMEC breast
9 chr21:46822600-46822800 Bivalent Enhancer Foreskin Keratinocyte Primary Cells skin03 Skin
10 chr21:46822600-46822800 Bivalent Enhancer HepG2 liver
11 chr21:46822600-46823000 Enhancers NHEK skin
12 chr21:46822600-46823400 Enhancers ES-WA7 Cell Line embryonic stem cell
13 chr21:46822600-46824000 Enhancers HUES6 Cell Line embryonic stem cell
14 chr21:46822600-46824000 Weak transcription Foreskin Melanocyte Primary Cells skin01 Skin
15 chr21:46822600-46824600 Enhancers Breast variant Human Mammary Epithelial Cells (vHMEC) Breast

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