Variant report

Variant rs73462348
Chromosome Location chr13:38973640-38973641
allele C/T
Outlinks Ensembl   UCSC
Chromatin state (count:12 , 50 per page) page: 1
No. Chromosome Location Chromatin state Cell line Tissue
1 chr13:38969800-38975400 Weak transcription Fetal Kidney kidney
2 chr13:38970000-38973800 Weak transcription Foreskin Fibroblast Primary Cells skin01 Skin
3 chr13:38972800-38973800 Enhancers Hela-S3 cervix
4 chr13:38972800-38974000 Enhancers Adipose Derived Mesenchymal Stem Cell Cultured Cells ES cell derived
5 chr13:38972800-38974000 Enhancers Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells embryonic stem cell
6 chr13:38972800-38974400 Enhancers Muscle Satellite Cultured Cells --
7 chr13:38973000-38974000 Enhancers HMEC breast
8 chr13:38973000-38974200 Enhancers Ovary ovary
9 chr13:38973000-38974400 Enhancers Fetal Adrenal Gland Adrenal Gland
10 chr13:38973000-38974400 Enhancers Fetal Lung lung
11 chr13:38973200-38974200 Enhancers NHDF-Ad bronchial
12 chr13:38973400-38974400 Enhancers Fetal Stomach stomach

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