Variant report

Variant rs4733657
Chromosome Location chr8:129901652-129901653
allele A/G
Outlinks Ensembl   UCSC
Chromatin state (count:10 , 50 per page) page: 1
No. Chromosome Location Chromatin state Cell line Tissue
1 chr8:129896400-129902400 Weak transcription HSMM muscle
2 chr8:129896400-129902800 Weak transcription Bone Marrow Derived Cultured Mesenchymal Stem Cells Bone marrow
3 chr8:129896400-129902800 Weak transcription Osteobl bone
4 chr8:129896800-129902800 Weak transcription Foreskin Fibroblast Primary Cells skin01 Skin
5 chr8:129896800-129903200 Weak transcription Foreskin Keratinocyte Primary Cells skin03 Skin
6 chr8:129898200-129903200 Weak transcription Breast variant Human Mammary Epithelial Cells (vHMEC) Breast
7 chr8:129899600-129909800 Weak transcription Dnd41 blood
8 chr8:129900600-129902800 Weak transcription Mesenchymal Stem Cell Derived Adipocyte Cultured Cells ES cell derived
9 chr8:129900600-129902800 Weak transcription NHDF-Ad bronchial
10 chr8:129901000-129901800 Enhancers Fetal Thymus thymus

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