Variant report

Variant rs1815697
Chromosome Location chr9:15877166-15877167
allele C/T
Outlinks Ensembl   UCSC
Chromatin state (count:9 , 50 per page) page: 1
No. Chromosome Location Chromatin state Cell line Tissue
1 chr9:15857800-15885400 Weak transcription Primary hematopoietic stem cells blood
2 chr9:15863600-15878200 Weak transcription Primary hematopoietic stem cells G-CSF-mobilized Male --
3 chr9:15874600-15878400 Weak transcription HSMMtube muscle
4 chr9:15876400-15877400 Strong transcription Foreskin Melanocyte Primary Cells skin03 Skin
5 chr9:15876600-15877200 Enhancers Adipose Derived Mesenchymal Stem Cell Cultured Cells ES cell derived
6 chr9:15876600-15877400 Enhancers Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells embryonic stem cell
7 chr9:15876800-15877200 Enhancers Foreskin Fibroblast Primary Cells skin01 Skin
8 chr9:15877000-15877200 Enhancers Muscle Satellite Cultured Cells --
9 chr9:15877000-15903400 Weak transcription Breast variant Human Mammary Epithelial Cells (vHMEC) Breast

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