Variant report

Variant rs73678294
Chromosome Location chr8:49390411-49390412
allele A/G
Outlinks Ensembl   UCSC
Chromatin state (count:8 , 50 per page) page: 1
No. Chromosome Location Chromatin state Cell line Tissue
1 chr8:49386800-49390800 Weak transcription NHLF lung
2 chr8:49386800-49391400 Weak transcription Foreskin Fibroblast Primary Cells skin02 Skin
3 chr8:49386800-49394600 Weak transcription Breast variant Human Mammary Epithelial Cells (vHMEC) Breast
4 chr8:49388200-49390600 Enhancers Fetal Muscle Trunk muscle
5 chr8:49389000-49391600 Weak transcription H1 Derived Mesenchymal Stem Cells ES cell derived
6 chr8:49390200-49390800 ZNF genes & repeats Foreskin Fibroblast Primary Cells skin01 Skin
7 chr8:49390200-49391000 ZNF genes & repeats H1 BMP4 Derived Trophoblast Cultured Cells ES cell derived
8 chr8:49390400-49390800 Enhancers iPS DF 19.11 Cell Line embryonic stem cell

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