Variant report

Variant rs11990598
Chromosome Location chr8:49389493-49389494
allele A/T
Outlinks Ensembl   UCSC
Chromatin state (count:9 , 50 per page) page: 1
No. Chromosome Location Chromatin state Cell line Tissue
1 chr8:49380200-49390400 Weak transcription iPS DF 19.11 Cell Line embryonic stem cell
2 chr8:49386800-49390200 Weak transcription H1 BMP4 Derived Trophoblast Cultured Cells ES cell derived
3 chr8:49386800-49390800 Weak transcription NHLF lung
4 chr8:49386800-49391400 Weak transcription Foreskin Fibroblast Primary Cells skin02 Skin
5 chr8:49386800-49394600 Weak transcription Breast variant Human Mammary Epithelial Cells (vHMEC) Breast
6 chr8:49387000-49390200 Weak transcription Foreskin Fibroblast Primary Cells skin01 Skin
7 chr8:49388200-49390600 Enhancers Fetal Muscle Trunk muscle
8 chr8:49389000-49391600 Weak transcription H1 Derived Mesenchymal Stem Cells ES cell derived
9 chr8:49389200-49389600 Enhancers Adipose Nuclei Adipose

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