Variant report

Variant rs115566063
Chromosome Location chr21:47208183-47208184
allele C/T
Outlinks Ensembl   UCSC
Chromatin state (count:10 , 50 per page) page: 1
No. Chromosome Location Chromatin state Cell line Tissue
1 chr21:47197400-47214200 Weak transcription Primary T cells from cord blood blood
2 chr21:47199200-47212800 Weak transcription Fetal Thymus thymus
3 chr21:47199400-47217200 Weak transcription Spleen Spleen
4 chr21:47206200-47208200 Enhancers Primary neutrophils fromperipheralblood blood
5 chr21:47208000-47208200 Bivalent Enhancer Fetal Muscle Trunk muscle
6 chr21:47208000-47208600 Bivalent Enhancer Foreskin Fibroblast Primary Cells skin02 Skin
7 chr21:47208000-47209000 Enhancers H1 Derived Mesenchymal Stem Cells ES cell derived
8 chr21:47208000-47209400 Enhancers NHDF-Ad bronchial
9 chr21:47208000-47213400 Strong transcription Thymus Thymus
10 chr21:47208000-47217200 Weak transcription H1 Derived Neuronal Progenitor Cultured Cells ES cell derived

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