Variant report

Variant rs140462109
Chromosome Location chr12:57293615-57293616
allele G/T
Outlinks Ensembl   UCSC
Chromatin state (count:15 , 50 per page) page: 1
No. Chromosome Location Chromatin state Cell line Tissue
1 chr12:57291000-57295600 Enhancers HMEC breast
2 chr12:57291200-57295800 Enhancers Breast variant Human Mammary Epithelial Cells (vHMEC) Breast
3 chr12:57291800-57296800 Enhancers K562 blood
4 chr12:57292600-57294600 Weak transcription Adipose Derived Mesenchymal Stem Cell Cultured Cells ES cell derived
5 chr12:57292800-57293800 Weak transcription Foreskin Keratinocyte Primary Cells skin03 Skin
6 chr12:57293600-57293800 Flanking Active TSS Liver Liver
7 chr12:57293600-57294400 ZNF genes & repeats Foreskin Keratinocyte Primary Cells skin02 Skin
8 chr12:57293600-57294600 ZNF genes & repeats iPS DF 19.11 Cell Line embryonic stem cell
9 chr12:57293600-57294800 ZNF genes & repeats H1 BMP4 Derived Trophoblast Cultured Cells ES cell derived
10 chr12:57293600-57294800 ZNF genes & repeats H1 Derived Mesenchymal Stem Cells ES cell derived
11 chr12:57293600-57294800 ZNF genes & repeats Foreskin Melanocyte Primary Cells skin01 Skin
12 chr12:57293600-57294800 ZNF genes & repeats Gastric stomach
13 chr12:57293600-57295200 ZNF genes & repeats Lung lung
14 chr12:57293600-57295200 ZNF genes & repeats NHEK skin
15 chr12:57293600-57295600 ZNF genes & repeats ES-UCSF4 Cell Line embryonic stem cell

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