Variant report

Variant rs2839078
Chromosome Location chr21:47429769-47429770
allele C/G
Outlinks Ensembl   UCSC
Chromatin state (count:18 , 50 per page) page: 1
No. Chromosome Location Chromatin state Cell line Tissue
1 chr21:47411200-47432800 Weak transcription Right Atrium heart
2 chr21:47422800-47438800 Weak transcription Colon Smooth Muscle Colon
3 chr21:47424000-47432800 Weak transcription iPS DF 6.9 Cell Line embryonic stem cell
4 chr21:47424600-47434400 Weak transcription Aorta Aorta
5 chr21:47424800-47430200 Weak transcription Fetal Brain Female brain
6 chr21:47424800-47431400 Weak transcription Right Ventricle heart
7 chr21:47425200-47431600 Weak transcription Adipose Derived Mesenchymal Stem Cell Cultured Cells ES cell derived
8 chr21:47425200-47431600 Weak transcription NHDF-Ad bronchial
9 chr21:47425200-47432400 Weak transcription Bone Marrow Derived Cultured Mesenchymal Stem Cells Bone marrow
10 chr21:47425400-47432200 Weak transcription Mesenchymal Stem Cell Derived Adipocyte Cultured Cells ES cell derived
11 chr21:47427600-47431600 Weak transcription H1 Derived Mesenchymal Stem Cells ES cell derived
12 chr21:47428600-47432000 Enhancers Foreskin Fibroblast Primary Cells skin02 Skin
13 chr21:47428800-47432000 Enhancers Ovary ovary
14 chr21:47429200-47430000 Enhancers Fetal Stomach stomach
15 chr21:47429400-47429800 Weak transcription Foreskin Fibroblast Primary Cells skin01 Skin
16 chr21:47429400-47430600 Enhancers Fetal Lung lung
17 chr21:47429400-47430600 Enhancers Fetal Muscle Trunk muscle
18 chr21:47429600-47431200 Weak transcription iPS DF 19.11 Cell Line embryonic stem cell

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