Variant report

Variant rs527263670
Chromosome Location chr21:28200241-28200242
allele G/T
Outlinks Ensembl   UCSC
Chromatin state (count:13 , 50 per page) page: 1
No. Chromosome Location Chromatin state Cell line Tissue
1 chr21:28198800-28200600 Enhancers Foreskin Keratinocyte Primary Cells skin03 Skin
2 chr21:28199000-28200600 Enhancers HMEC breast
3 chr21:28199000-28208400 Weak transcription ES-UCSF4 Cell Line embryonic stem cell
4 chr21:28199200-28200600 Enhancers Breast Myoepithelial Primary Cells Breast
5 chr21:28199200-28200600 Enhancers Foreskin Keratinocyte Primary Cells skin02 Skin
6 chr21:28199200-28208800 Weak transcription IMR90 fetal lung fibroblasts Cell Line lung
7 chr21:28199400-28200600 Enhancers NHEK skin
8 chr21:28199400-28203600 Weak transcription Primary Natural Killer cells fromperipheralblood blood
9 chr21:28199400-28205600 Weak transcription H1 Derived Mesenchymal Stem Cells ES cell derived
10 chr21:28199800-28200600 Enhancers Breast variant Human Mammary Epithelial Cells (vHMEC) Breast
11 chr21:28199800-28200600 Enhancers Dnd41 blood
12 chr21:28199800-28205200 Weak transcription Muscle Satellite Cultured Cells --
13 chr21:28199800-28208800 Weak transcription hESC Derived CD184+ Endoderm Cultured Cells ES cell derived

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