Variant report

Variant rs6798469
Chromosome Location chr3:139901534-139901535
allele C/T
Outlinks Ensembl   UCSC
Chromatin state (count:13 , 50 per page) page: 1
No. Chromosome Location Chromatin state Cell line Tissue
1 chr3:139898800-139901800 Enhancers Skeletal Muscle Female skeletal muscle
2 chr3:139899200-139904600 Weak transcription HSMMtube muscle
3 chr3:139900000-139904400 Weak transcription Breast Myoepithelial Primary Cells Breast
4 chr3:139900000-139904600 Weak transcription Foreskin Keratinocyte Primary Cells skin02 Skin
5 chr3:139900000-139904600 Weak transcription Adipose Nuclei Adipose
6 chr3:139900000-139904600 Weak transcription NHDF-Ad bronchial
7 chr3:139900000-139904800 Weak transcription NHEK skin
8 chr3:139900000-139905800 Weak transcription Esophagus oesophagus
9 chr3:139900200-139904800 Weak transcription Breast variant Human Mammary Epithelial Cells (vHMEC) Breast
10 chr3:139901200-139901600 ZNF genes & repeats H1 BMP4 Derived Trophoblast Cultured Cells ES cell derived
11 chr3:139901200-139901800 Strong transcription H1 Derived Mesenchymal Stem Cells ES cell derived
12 chr3:139901200-139901800 Enhancers Psoas Muscle Psoas
13 chr3:139901400-139904400 Weak transcription Right Atrium heart

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