Variant report

Variant rs12345852
Chromosome Location chr9:110650815-110650816
allele A/G
Outlinks Ensembl   UCSC
Chromatin state (count:13 , 50 per page) page: 1
No. Chromosome Location Chromatin state Cell line Tissue
1 chr9:110635800-110656800 Weak transcription H9 Cell Line embryonic stem cell
2 chr9:110644400-110651000 Weak transcription Adipose Derived Mesenchymal Stem Cell Cultured Cells ES cell derived
3 chr9:110644800-110658800 Weak transcription Breast variant Human Mammary Epithelial Cells (vHMEC) Breast
4 chr9:110646200-110651000 Weak transcription Fetal Muscle Leg muscle
5 chr9:110646400-110651000 Weak transcription Foreskin Fibroblast Primary Cells skin01 Skin
6 chr9:110646800-110652600 Weak transcription H1 Derived Mesenchymal Stem Cells ES cell derived
7 chr9:110649200-110651000 Weak transcription Right Atrium heart
8 chr9:110649200-110657000 Weak transcription iPS DF 19.11 Cell Line embryonic stem cell
9 chr9:110649400-110651000 Weak transcription Ovary ovary
10 chr9:110649800-110651000 Weak transcription Skeletal Muscle Female skeletal muscle
11 chr9:110650600-110652200 Enhancers Mesenchymal Stem Cell Derived Adipocyte Cultured Cells ES cell derived
12 chr9:110650800-110651800 Enhancers Bone Marrow Derived Cultured Mesenchymal Stem Cells Bone marrow
13 chr9:110650800-110651800 Enhancers Adipose Nuclei Adipose

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