Variant report

Variant rs28903677
Chromosome Location chr2:234944729-234944730
allele A/C
Outlinks Ensembl   UCSC
Chromatin state (count:7 , 50 per page) page: 1
No. Chromosome Location Chromatin state Cell line Tissue
1 chr2:234941800-234952600 Weak transcription Breast variant Human Mammary Epithelial Cells (vHMEC) Breast
2 chr2:234942200-234945000 Weak transcription Foreskin Fibroblast Primary Cells skin02 Skin
3 chr2:234943400-234946200 Weak transcription Primary T helper memory cells from peripheral blood 1 blood
4 chr2:234943800-234944800 ZNF genes & repeats H1 Derived Mesenchymal Stem Cells ES cell derived
5 chr2:234943800-234944800 ZNF genes & repeats Foreskin Fibroblast Primary Cells skin01 Skin
6 chr2:234944000-234944800 Bivalent Enhancer Primary T cells fromperipheralblood blood
7 chr2:234944000-234946200 Weak transcription Foreskin Melanocyte Primary Cells skin03 Skin

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