Variant report

Variant rs9620793
Chromosome Location chr22:21428952-21428953
allele A/G
Outlinks Ensembl   UCSC
Chromatin state (count:19 , 50 per page) page: 1
No. Chromosome Location Chromatin state Cell line Tissue
1 chr22:21423000-21429200 Enhancers Placenta Placenta
2 chr22:21427000-21429000 Enhancers NHEK skin
3 chr22:21427200-21429000 Enhancers HMEC breast
4 chr22:21427200-21429200 Enhancers Breast variant Human Mammary Epithelial Cells (vHMEC) Breast
5 chr22:21427400-21429000 Enhancers Foreskin Keratinocyte Primary Cells skin03 Skin
6 chr22:21427600-21429000 Enhancers NHLF lung
7 chr22:21427600-21435600 Strong transcription Right Atrium heart
8 chr22:21427800-21429000 Enhancers NHDF-Ad bronchial
9 chr22:21427800-21429000 Enhancers Osteobl bone
10 chr22:21428000-21429000 Enhancers NH-A brain
11 chr22:21428000-21429200 Enhancers Muscle Satellite Cultured Cells --
12 chr22:21428200-21429000 Enhancers IMR90 fetal lung fibroblasts Cell Line lung
13 chr22:21428200-21429000 Enhancers Adipose Derived Mesenchymal Stem Cell Cultured Cells ES cell derived
14 chr22:21428200-21429000 Enhancers Bone Marrow Derived Cultured Mesenchymal Stem Cells Bone marrow
15 chr22:21428200-21429200 Enhancers Foreskin Fibroblast Primary Cells skin01 Skin
16 chr22:21428200-21429200 Enhancers HSMM muscle
17 chr22:21428400-21429200 Enhancers Hela-S3 cervix
18 chr22:21428600-21434800 Weak transcription iPS DF 19.11 Cell Line embryonic stem cell
19 chr22:21428800-21435000 Weak transcription H1 Derived Mesenchymal Stem Cells ES cell derived

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