Variant report

Variant rs55912352
Chromosome Location chr21:47273127-47273128
allele A/G
Outlinks Ensembl   UCSC
Chromatin state (count:17 , 50 per page) page: 1
No. Chromosome Location Chromatin state Cell line Tissue
1 chr21:47261800-47275200 Weak transcription iPS-20b Cell Line embryonic stem cell
2 chr21:47263800-47274400 Weak transcription Spleen Spleen
3 chr21:47264000-47275000 Weak transcription H9 Cell Line embryonic stem cell
4 chr21:47265800-47274400 Weak transcription HSMMtube muscle
5 chr21:47265800-47282000 Weak transcription Primary T cells from cord blood blood
6 chr21:47266800-47300600 Weak transcription Right Atrium heart
7 chr21:47268200-47273600 Weak transcription Breast Myoepithelial Primary Cells Breast
8 chr21:47269800-47274800 Weak transcription H1 Derived Mesenchymal Stem Cells ES cell derived
9 chr21:47270600-47274000 Weak transcription iPS DF 19.11 Cell Line embryonic stem cell
10 chr21:47271600-47273200 Weak transcription Primary neutrophils fromperipheralblood blood
11 chr21:47272400-47273200 Strong transcription Mesenchymal Stem Cell Derived Adipocyte Cultured Cells ES cell derived
12 chr21:47272400-47282000 Strong transcription Thymus Thymus
13 chr21:47272600-47273200 Strong transcription IMR90 fetal lung fibroblasts Cell Line lung
14 chr21:47272600-47273200 ZNF genes & repeats Aorta Aorta
15 chr21:47272600-47273600 Strong transcription Adipose Derived Mesenchymal Stem Cell Cultured Cells ES cell derived
16 chr21:47272800-47275400 Genic enhancers Fetal Thymus thymus
17 chr21:47273000-47273400 Enhancers Brain Hippocampus Middle brain

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