Variant report

Variant rs13016940
Chromosome Location chr2:133302224-133302225
allele C/T
Outlinks Ensembl   UCSC
Chromatin state (count:10 , 50 per page) page: 1
No. Chromosome Location Chromatin state Cell line Tissue
1 chr2:133299000-133303400 ZNF genes & repeats hESC Derived CD184+ Endoderm Cultured Cells ES cell derived
2 chr2:133299200-133302800 Enhancers Placenta Placenta
3 chr2:133300400-133302400 ZNF genes & repeats Liver Liver
4 chr2:133300600-133302600 ZNF genes & repeats Foreskin Keratinocyte Primary Cells skin02 Skin
5 chr2:133301200-133303000 ZNF genes & repeats ES-UCSF4 Cell Line embryonic stem cell
6 chr2:133301400-133302400 Enhancers H1 Derived Mesenchymal Stem Cells ES cell derived
7 chr2:133301600-133308400 Weak transcription Breast variant Human Mammary Epithelial Cells (vHMEC) Breast
8 chr2:133302000-133302400 Flanking Bivalent TSS/Enh H1 BMP4 Derived Trophoblast Cultured Cells ES cell derived
9 chr2:133302000-133302400 ZNF genes & repeats iPS DF 6.9 Cell Line embryonic stem cell
10 chr2:133302000-133302800 ZNF genes & repeats Fetal Brain Female brain

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