Variant report

Variant rs3922514
Chromosome Location chr4:69926623-69926624
allele A/G
Outlinks Ensembl   UCSC
Chromatin state (count:10 , 50 per page) page: 1
No. Chromosome Location Chromatin state Cell line Tissue
1 chr4:69923800-69932400 Weak transcription Breast variant Human Mammary Epithelial Cells (vHMEC) Breast
2 chr4:69925000-69928800 Weak transcription Fetal Kidney kidney
3 chr4:69925000-69930000 Weak transcription Foreskin Melanocyte Primary Cells skin03 Skin
4 chr4:69925000-69932600 Weak transcription Foreskin Melanocyte Primary Cells skin01 Skin
5 chr4:69925600-69927400 Enhancers Liver Liver
6 chr4:69925800-69929600 ZNF genes & repeats H1 Derived Mesenchymal Stem Cells ES cell derived
7 chr4:69926400-69927200 Enhancers Pancreas Pancrea
8 chr4:69926600-69926800 Enhancers iPS-15b Cell Line embryonic stem cell
9 chr4:69926600-69927400 Enhancers Stomach Mucosa stomach
10 chr4:69926600-69927800 Genic enhancers HepG2 liver

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