Variant report

Variant rs7869376
Chromosome Location chr9:72118434-72118435
allele C/T
Outlinks Ensembl   UCSC
Chromatin state (count:14 , 50 per page) page: 1
No. Chromosome Location Chromatin state Cell line Tissue
1 chr9:72107800-72130000 Weak transcription Pancreas Pancrea
2 chr9:72114200-72130000 Weak transcription Breast Myoepithelial Primary Cells Breast
3 chr9:72114800-72128200 Weak transcription Fetal Adrenal Gland Adrenal Gland
4 chr9:72116000-72119000 Enhancers Primary T helper 17 cells PMA-I stimulated --
5 chr9:72117600-72118600 Enhancers Adipose Derived Mesenchymal Stem Cell Cultured Cells ES cell derived
6 chr9:72117600-72118600 Enhancers NHDF-Ad bronchial
7 chr9:72117600-72118800 Enhancers Muscle Satellite Cultured Cells --
8 chr9:72117600-72118800 Enhancers NHEK skin
9 chr9:72117800-72118800 Enhancers Foreskin Fibroblast Primary Cells skin02 Skin
10 chr9:72118000-72120200 Weak transcription HMEC breast
11 chr9:72118200-72119600 Enhancers Liver Liver
12 chr9:72118400-72119400 Enhancers HUVEC blood vessel
13 chr9:72118400-72119600 Weak transcription Breast variant Human Mammary Epithelial Cells (vHMEC) Breast
14 chr9:72118400-72120000 Weak transcription Foreskin Keratinocyte Primary Cells skin02 Skin

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