Variant report

Variant rs1721039
Chromosome Location chr7:16990890-16990891
allele C/G
Outlinks Ensembl   UCSC
Chromatin state (count:8 , 50 per page) page: 1
No. Chromosome Location Chromatin state Cell line Tissue
1 chr7:16988600-16991400 Weak transcription Fetal Stomach stomach
2 chr7:16988600-16991800 Weak transcription H1 BMP4 Derived Trophoblast Cultured Cells ES cell derived
3 chr7:16988600-17009000 Weak transcription Breast variant Human Mammary Epithelial Cells (vHMEC) Breast
4 chr7:16990200-16991600 Enhancers Foreskin Melanocyte Primary Cells skin03 Skin
5 chr7:16990400-16991000 Enhancers Foreskin Melanocyte Primary Cells skin01 Skin
6 chr7:16990800-16991200 Enhancers Bone Marrow Derived Cultured Mesenchymal Stem Cells Bone marrow
7 chr7:16990800-16991200 Enhancers Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells embryonic stem cell
8 chr7:16990800-16991400 Weak transcription Breast Myoepithelial Primary Cells Breast

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