Variant report

Variant rs73955478
Chromosome Location chr2:114780155-114780156
allele A/G
Outlinks Ensembl   UCSC
Chromatin state (count:15 , 50 per page) page: 1
No. Chromosome Location Chromatin state Cell line Tissue
1 chr2:114778400-114786400 Weak transcription Pancreas Pancrea
2 chr2:114779200-114780600 Enhancers HepG2 liver
3 chr2:114779400-114781400 Enhancers HMEC breast
4 chr2:114779400-114782000 Enhancers Adipose Derived Mesenchymal Stem Cell Cultured Cells ES cell derived
5 chr2:114779600-114780600 Enhancers Breast variant Human Mammary Epithelial Cells (vHMEC) Breast
6 chr2:114779600-114780800 Enhancers Bone Marrow Derived Cultured Mesenchymal Stem Cells Bone marrow
7 chr2:114779600-114780800 Enhancers Foreskin Keratinocyte Primary Cells skin03 Skin
8 chr2:114779600-114780800 Enhancers NHEK skin
9 chr2:114779600-114781400 Enhancers Osteobl bone
10 chr2:114779600-114781600 Enhancers NHLF lung
11 chr2:114779800-114780800 Enhancers Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells embryonic stem cell
12 chr2:114779800-114780800 Enhancers Muscle Satellite Cultured Cells --
13 chr2:114779800-114780800 Enhancers NHDF-Ad bronchial
14 chr2:114779800-114781200 Enhancers Foreskin Keratinocyte Primary Cells skin02 Skin
15 chr2:114780000-114780200 Enhancers NH-A brain

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