Variant report

Variant rs12375636
Chromosome Location chr9:102941591-102941592
allele A/G
Outlinks Ensembl   UCSC
Chromatin state (count:11 , 50 per page) page: 1
No. Chromosome Location Chromatin state Cell line Tissue
1 chr9:102933400-102942000 Weak transcription Muscle Satellite Cultured Cells --
2 chr9:102935400-102952000 Weak transcription Small Intestine intestine
3 chr9:102936200-102941600 Weak transcription Foreskin Fibroblast Primary Cells skin02 Skin
4 chr9:102936400-102952600 Weak transcription Breast variant Human Mammary Epithelial Cells (vHMEC) Breast
5 chr9:102937800-102952000 Weak transcription H1 Derived Mesenchymal Stem Cells ES cell derived
6 chr9:102938400-102950600 Weak transcription Liver Liver
7 chr9:102939600-102950800 Weak transcription Ovary ovary
8 chr9:102940200-102952000 Weak transcription Pancreas Pancrea
9 chr9:102940200-102959200 Weak transcription H1 BMP4 Derived Trophoblast Cultured Cells ES cell derived
10 chr9:102940400-102959200 Weak transcription Foreskin Keratinocyte Primary Cells skin03 Skin
11 chr9:102940400-102978000 Weak transcription Foreskin Keratinocyte Primary Cells skin02 Skin

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