Variant report

Variant rs11177067
Chromosome Location chr12:68526887-68526888
allele C/T
Outlinks Ensembl   UCSC
Chromatin state (count:12 , 50 per page) page: 1
No. Chromosome Location Chromatin state Cell line Tissue
1 chr12:68524200-68530000 Weak transcription iPS DF 19.11 Cell Line embryonic stem cell
2 chr12:68525200-68530200 Weak transcription Primary T cells from cord blood blood
3 chr12:68525600-68527000 Enhancers Foreskin Keratinocyte Primary Cells skin02 Skin
4 chr12:68525600-68527000 Enhancers HMEC breast
5 chr12:68525600-68527000 Enhancers NHEK skin
6 chr12:68525600-68527200 Enhancers Breast variant Human Mammary Epithelial Cells (vHMEC) Breast
7 chr12:68525800-68527000 Enhancers Placenta Placenta
8 chr12:68526000-68527200 Enhancers H1 BMP4 Derived Trophoblast Cultured Cells ES cell derived
9 chr12:68526200-68527000 Enhancers Esophagus oesophagus
10 chr12:68526200-68528000 Enhancers Foreskin Melanocyte Primary Cells skin01 Skin
11 chr12:68526400-68527400 Enhancers Foreskin Melanocyte Primary Cells skin03 Skin
12 chr12:68526400-68529800 Weak transcription Primary T killer naive cells fromperipheralblood blood

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