Variant report

Variant rs35888804
Chromosome Location chr9:96887153-96887154
allele C/T
Outlinks Ensembl   UCSC
Chromatin state (count:11 , 50 per page) page: 1
No. Chromosome Location Chromatin state Cell line Tissue
1 chr9:96867600-96889600 Weak transcription Foreskin Melanocyte Primary Cells skin01 Skin
2 chr9:96871400-96896400 Weak transcription Skeletal Muscle Male skeletal muscle
3 chr9:96873400-96888600 Weak transcription HSMM muscle
4 chr9:96874200-96896400 Weak transcription Breast variant Human Mammary Epithelial Cells (vHMEC) Breast
5 chr9:96875400-96887200 Weak transcription Brain Anterior Caudate brain
6 chr9:96881800-96896000 Weak transcription Left Ventricle heart
7 chr9:96883400-96896800 Weak transcription Foreskin Fibroblast Primary Cells skin02 Skin
8 chr9:96884200-96888400 Weak transcription Primary T helper naive cells fromperipheralblood blood
9 chr9:96884200-96888800 Weak transcription Brain Angular Gyrus brain
10 chr9:96886800-96887200 Weak transcription Foreskin Melanocyte Primary Cells skin03 Skin
11 chr9:96886800-96887400 Strong transcription Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells embryonic stem cell

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