Variant report

Variant rs34928385
Chromosome Location chr16:76710297-76710298
allele -/G
Outlinks Ensembl   UCSC
Chromatin state (count:14 , 50 per page) page: 1
No. Chromosome Location Chromatin state Cell line Tissue
1 chr16:76696600-76714800 Weak transcription H1 BMP4 Derived Mesendoderm Cultured Cells ES cell derived
2 chr16:76708000-76710800 Enhancers iPS-20b Cell Line embryonic stem cell
3 chr16:76708600-76711400 Enhancers Placenta Amnion Placenta Amnion
4 chr16:76708800-76710800 Enhancers H1 BMP4 Derived Trophoblast Cultured Cells ES cell derived
5 chr16:76709200-76711200 Enhancers Breast variant Human Mammary Epithelial Cells (vHMEC) Breast
6 chr16:76709200-76711400 Enhancers HMEC breast
7 chr16:76709400-76711000 Enhancers Adipose Derived Mesenchymal Stem Cell Cultured Cells ES cell derived
8 chr16:76709400-76711400 Enhancers Placenta Placenta
9 chr16:76709800-76710600 Enhancers HUES64 Cell Line embryonic stem cell
10 chr16:76710000-76710800 Enhancers H9 Cell Line embryonic stem cell
11 chr16:76710200-76710800 Enhancers HUES48 Cell Line embryonic stem cell
12 chr16:76710200-76710800 Enhancers HUES6 Cell Line embryonic stem cell
13 chr16:76710200-76710800 Enhancers iPS-18 Cell Line embryonic stem cell
14 chr16:76710200-76710800 Enhancers Foreskin Keratinocyte Primary Cells skin02 Skin

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