Variant report

Variant rs403653
Chromosome Location chr22:21427577-21427578
allele A/G
Outlinks Ensembl   UCSC
Chromatin state (count:11 , 50 per page) page: 1
No. Chromosome Location Chromatin state Cell line Tissue
1 chr22:21423000-21429200 Enhancers Placenta Placenta
2 chr22:21425800-21428400 Weak transcription iPS DF 19.11 Cell Line embryonic stem cell
3 chr22:21426000-21427600 Weak transcription Right Atrium heart
4 chr22:21426800-21428600 Enhancers Esophagus oesophagus
5 chr22:21427000-21429000 Enhancers NHEK skin
6 chr22:21427200-21428600 Enhancers Foreskin Keratinocyte Primary Cells skin02 Skin
7 chr22:21427200-21429000 Enhancers HMEC breast
8 chr22:21427200-21429200 Enhancers Breast variant Human Mammary Epithelial Cells (vHMEC) Breast
9 chr22:21427400-21427800 Enhancers Breast Myoepithelial Primary Cells Breast
10 chr22:21427400-21428200 Weak transcription H1 Derived Mesenchymal Stem Cells ES cell derived
11 chr22:21427400-21429000 Enhancers Foreskin Keratinocyte Primary Cells skin03 Skin

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