Variant report

Variant rs538517168
Chromosome Location chr21:47497696-47497697
allele A/G
Outlinks Ensembl   UCSC
Chromatin state (count:10 , 50 per page) page: 1
No. Chromosome Location Chromatin state Cell line Tissue
1 chr21:47485200-47517400 Weak transcription Right Atrium heart
2 chr21:47488000-47498000 Weak transcription Foreskin Fibroblast Primary Cells skin01 Skin
3 chr21:47489400-47511000 Weak transcription iPS DF 6.9 Cell Line embryonic stem cell
4 chr21:47489600-47499200 Weak transcription iPS DF 19.11 Cell Line embryonic stem cell
5 chr21:47489600-47511000 Weak transcription H9 Cell Line embryonic stem cell
6 chr21:47491200-47499000 Weak transcription H1 Derived Mesenchymal Stem Cells ES cell derived
7 chr21:47492800-47498400 Weak transcription Mesenchymal Stem Cell Derived Adipocyte Cultured Cells ES cell derived
8 chr21:47497400-47498200 Enhancers Adipose Derived Mesenchymal Stem Cell Cultured Cells ES cell derived
9 chr21:47497600-47497800 Flanking Active TSS Foreskin Fibroblast Primary Cells skin02 Skin
10 chr21:47497600-47504800 Enhancers NHDF-Ad bronchial

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