Variant report

Variant rs12477192
Chromosome Location chr2:133300702-133300703
allele G/T
Outlinks Ensembl   UCSC
Chromatin state (count:14 , 50 per page) page: 1
No. Chromosome Location Chromatin state Cell line Tissue
1 chr2:133296600-133301400 Weak transcription H1 Derived Mesenchymal Stem Cells ES cell derived
2 chr2:133297400-133301000 Weak transcription Gastric stomach
3 chr2:133299000-133303400 ZNF genes & repeats hESC Derived CD184+ Endoderm Cultured Cells ES cell derived
4 chr2:133299200-133302800 Enhancers Placenta Placenta
5 chr2:133300200-133302000 Enhancers H1 BMP4 Derived Trophoblast Cultured Cells ES cell derived
6 chr2:133300400-133301000 Enhancers ES-WA7 Cell Line embryonic stem cell
7 chr2:133300400-133301000 Enhancers A549 lung
8 chr2:133300400-133301200 Enhancers Adipose Derived Mesenchymal Stem Cell Cultured Cells ES cell derived
9 chr2:133300400-133301400 Enhancers HMEC breast
10 chr2:133300400-133301400 ZNF genes & repeats NHEK skin
11 chr2:133300400-133302400 ZNF genes & repeats Liver Liver
12 chr2:133300600-133301200 ZNF genes & repeats Mesenchymal Stem Cell Derived Adipocyte Cultured Cells ES cell derived
13 chr2:133300600-133301200 Genic enhancers Breast variant Human Mammary Epithelial Cells (vHMEC) Breast
14 chr2:133300600-133302600 ZNF genes & repeats Foreskin Keratinocyte Primary Cells skin02 Skin

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