Variant report

Variant rs11987212
Chromosome Location chr8:49840154-49840155
allele A/G
Outlinks Ensembl   UCSC
Chromatin state (count:14 , 50 per page) page: 1
No. Chromosome Location Chromatin state Cell line Tissue
1 chr8:49835000-49840200 Enhancers Placenta Amnion Placenta Amnion
2 chr8:49836800-49843200 Weak transcription Esophagus oesophagus
3 chr8:49837800-49846200 Weak transcription Foreskin Melanocyte Primary Cells skin01 Skin
4 chr8:49838000-49841600 Weak transcription Breast Myoepithelial Primary Cells Breast
5 chr8:49838000-49841600 Weak transcription Breast variant Human Mammary Epithelial Cells (vHMEC) Breast
6 chr8:49838600-49843000 Weak transcription Osteobl bone
7 chr8:49838800-49841400 Weak transcription HMEC breast
8 chr8:49838800-49841600 Weak transcription Foreskin Keratinocyte Primary Cells skin03 Skin
9 chr8:49838800-49841800 Weak transcription NHEK skin
10 chr8:49838800-49842000 Weak transcription Foreskin Keratinocyte Primary Cells skin02 Skin
11 chr8:49838800-49843000 Weak transcription Adipose Derived Mesenchymal Stem Cell Cultured Cells ES cell derived
12 chr8:49839600-49842000 Weak transcription Primary B cells from peripheral blood blood
13 chr8:49840000-49840200 ZNF genes & repeats H1 BMP4 Derived Trophoblast Cultured Cells ES cell derived
14 chr8:49840000-49840800 Enhancers Thymus Thymus

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