Variant report

Variant rs9798612
Chromosome Location chr21:47468327-47468328
allele A/G
Outlinks Ensembl   UCSC
Chromatin state (count:18 , 50 per page) page: 1
No. Chromosome Location Chromatin state Cell line Tissue
1 chr21:47459400-47468600 Weak transcription HSMMtube muscle
2 chr21:47461400-47468600 Weak transcription Foreskin Fibroblast Primary Cells skin01 Skin
3 chr21:47461400-47468800 Weak transcription H1 Derived Mesenchymal Stem Cells ES cell derived
4 chr21:47463400-47468800 Weak transcription ES-I3 Cell Line embryonic stem cell
5 chr21:47465200-47468400 Weak transcription Osteobl bone
6 chr21:47465600-47468600 Weak transcription Bone Marrow Derived Cultured Mesenchymal Stem Cells Bone marrow
7 chr21:47466000-47468600 Weak transcription Mesenchymal Stem Cell Derived Adipocyte Cultured Cells ES cell derived
8 chr21:47466800-47468400 Weak transcription NHLF lung
9 chr21:47466800-47468800 Weak transcription IMR90 fetal lung fibroblasts Cell Line lung
10 chr21:47466800-47468800 Weak transcription Foreskin Fibroblast Primary Cells skin02 Skin
11 chr21:47467000-47469000 Weak transcription iPS DF 19.11 Cell Line embryonic stem cell
12 chr21:47468000-47472600 Enhancers Fetal Lung lung
13 chr21:47468200-47469000 Enhancers Placenta Placenta
14 chr21:47468200-47470400 Enhancers Colonic Mucosa Colon
15 chr21:47468200-47470400 Enhancers Fetal Stomach stomach
16 chr21:47468200-47471600 Enhancers Adipose Derived Mesenchymal Stem Cell Cultured Cells ES cell derived
17 chr21:47468200-47477800 Enhancers NHDF-Ad bronchial
18 chr21:47468200-47478000 Enhancers Fetal Muscle Leg muscle

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