Variant report

Variant esv1814277
Chromosome Location chr21:47343676-47345261
allele n/a
Outlinks Ensembl   UCSC
Chromatin state (count:14 , 50 per page) page: 1
No. Chromosome Location Chromatin state Cell line Tissue
1 chr21:47333600-47351600 Weak transcription Gastric stomach
2 chr21:47340000-47354800 Weak transcription Primary T cells from cord blood blood
3 chr21:47342600-47343800 Enhancers Adipose Derived Mesenchymal Stem Cell Cultured Cells ES cell derived
4 chr21:47342600-47344200 ZNF genes & repeats iPS DF 19.11 Cell Line embryonic stem cell
5 chr21:47343200-47343800 Enhancers Foreskin Fibroblast Primary Cells skin02 Skin
6 chr21:47343200-47350400 Weak transcription Spleen Spleen
7 chr21:47343400-47353800 Weak transcription H1 Derived Mesenchymal Stem Cells ES cell derived
8 chr21:47343600-47343800 Weak transcription Primary T cells fromperipheralblood blood
9 chr21:47343600-47346800 Weak transcription Fetal Muscle Leg muscle
10 chr21:47343600-47347400 Weak transcription Primary T helper cells fromperipheralblood blood
11 chr21:47343600-47353600 Weak transcription Brain Hippocampus Middle brain
12 chr21:47343600-47354600 Weak transcription Mesenchymal Stem Cell Derived Adipocyte Cultured Cells ES cell derived
13 chr21:47344000-47344400 ZNF genes & repeats Esophagus oesophagus
14 chr21:47345200-47346000 Weak transcription iPS DF 19.11 Cell Line embryonic stem cell

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