Variant report

Variant rs58599510
Chromosome Location chr22:21427714-21427715
allele A/C
Outlinks Ensembl   UCSC
Chromatin state (count:13 , 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 chr22:21426800-21428600 Enhancers Esophagus oesophagus
4 chr22:21427000-21429000 Enhancers NHEK skin
5 chr22:21427200-21428600 Enhancers Foreskin Keratinocyte Primary Cells skin02 Skin
6 chr22:21427200-21429000 Enhancers HMEC breast
7 chr22:21427200-21429200 Enhancers Breast variant Human Mammary Epithelial Cells (vHMEC) Breast
8 chr22:21427400-21427800 Enhancers Breast Myoepithelial Primary Cells Breast
9 chr22:21427400-21428200 Weak transcription H1 Derived Mesenchymal Stem Cells ES cell derived
10 chr22:21427400-21429000 Enhancers Foreskin Keratinocyte Primary Cells skin03 Skin
11 chr22:21427600-21428800 Enhancers Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells embryonic stem cell
12 chr22:21427600-21429000 Enhancers NHLF lung
13 chr22:21427600-21435600 Strong transcription Right Atrium heart

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