Variant report

Variant rs28689568
Chromosome Location chr4:3912496-3912497
allele C/T
Outlinks Ensembl   UCSC
Chromatin state (count:10 , 50 per page) page: 1
No. Chromosome Location Chromatin state Cell line Tissue
1 chr4:3905200-3913000 Weak transcription iPS DF 19.11 Cell Line embryonic stem cell
2 chr4:3907200-3912800 Weak transcription H1 BMP4 Derived Trophoblast Cultured Cells ES cell derived
3 chr4:3911200-3913600 Enhancers NHDF-Ad bronchial
4 chr4:3911800-3912600 Enhancers Placenta Placenta
5 chr4:3911800-3913000 Enhancers Fetal Heart heart
6 chr4:3912000-3912600 Flanking Active TSS Foreskin Fibroblast Primary Cells skin01 Skin
7 chr4:3912000-3913000 Enhancers Adipose Derived Mesenchymal Stem Cell Cultured Cells ES cell derived
8 chr4:3912200-3912800 Enhancers Foreskin Fibroblast Primary Cells skin02 Skin
9 chr4:3912200-3913400 Enhancers Adipose Nuclei Adipose
10 chr4:3912400-3916200 Weak transcription Mesenchymal Stem Cell Derived Adipocyte Cultured Cells ES cell derived

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