Variant report

Variant rs571961926
Chromosome Location chr2:185550657-185550658
allele C/T
Outlinks Ensembl   UCSC
Chromatin state (count:10 , 50 per page) page: 1
No. Chromosome Location Chromatin state Cell line Tissue
1 chr2:185545200-185557000 Weak transcription Fetal Stomach stomach
2 chr2:185545800-185552200 Weak transcription iPS DF 6.9 Cell Line embryonic stem cell
3 chr2:185548600-185552200 Enhancers NHEK skin
4 chr2:185549000-185551000 Weak transcription Primary hematopoietic stem cells G-CSF-mobilized Male --
5 chr2:185550000-185550800 ZNF genes & repeats Foreskin Fibroblast Primary Cells skin02 Skin
6 chr2:185550200-185552000 Enhancers Foreskin Keratinocyte Primary Cells skin03 Skin
7 chr2:185550400-185551200 Enhancers Foreskin Keratinocyte Primary Cells skin02 Skin
8 chr2:185550600-185551000 Enhancers iPS DF 19.11 Cell Line embryonic stem cell
9 chr2:185550600-185551000 Enhancers HMEC breast
10 chr2:185550600-185551200 Enhancers H1 Derived Mesenchymal Stem Cells ES cell derived

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