Variant report

Variant rs4721552
Chromosome Location chr7:16995211-16995212
allele C/G
Outlinks Ensembl   UCSC
Chromatin state (count:11 , 50 per page) page: 1
No. Chromosome Location Chromatin state Cell line Tissue
1 chr7:16988600-17009000 Weak transcription Breast variant Human Mammary Epithelial Cells (vHMEC) Breast
2 chr7:16991200-17002200 Weak transcription Stomach Mucosa stomach
3 chr7:16992000-16995800 Weak transcription H1 Derived Neuronal Progenitor Cultured Cells ES cell derived
4 chr7:16992000-16999800 Weak transcription Bone Marrow Derived Cultured Mesenchymal Stem Cells Bone marrow
5 chr7:16992000-16999800 Weak transcription Osteobl bone
6 chr7:16993000-16995600 Enhancers Fetal Heart heart
7 chr7:16994000-16998000 Weak transcription HepG2 liver
8 chr7:16994200-16995400 Weak transcription NHDF-Ad bronchial
9 chr7:16994400-16999200 Weak transcription HSMMtube muscle
10 chr7:16994400-17000000 Weak transcription Mesenchymal Stem Cell Derived Adipocyte Cultured Cells ES cell derived
11 chr7:16994800-16999600 Weak transcription Adipose Derived Mesenchymal Stem Cell Cultured Cells ES cell derived

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