Variant report

Variant rs576832081
Chromosome Location chr2:55000198-55000199
allele C/T
Outlinks Ensembl   UCSC
Chromatin state (count:20 , 50 per page) page: 1
No. Chromosome Location Chromatin state Cell line Tissue
1 chr2:54997400-55000600 Enhancers Foreskin Fibroblast Primary Cells skin01 Skin
2 chr2:54997400-55000800 Enhancers HSMMtube muscle
3 chr2:54997600-55000600 Enhancers HSMM muscle
4 chr2:54997600-55000800 Enhancers HMEC breast
5 chr2:54997600-55001400 Enhancers Foreskin Keratinocyte Primary Cells skin03 Skin
6 chr2:54997800-55000600 Enhancers Breast variant Human Mammary Epithelial Cells (vHMEC) Breast
7 chr2:54997800-55000600 Enhancers Foreskin Keratinocyte Primary Cells skin02 Skin
8 chr2:54997800-55000600 Enhancers NHDF-Ad bronchial
9 chr2:54998000-55000200 Enhancers HUVEC blood vessel
10 chr2:54998000-55000600 Enhancers Muscle Satellite Cultured Cells --
11 chr2:54998200-55000400 Enhancers Foreskin Fibroblast Primary Cells skin02 Skin
12 chr2:54998200-55000400 Enhancers Osteobl bone
13 chr2:54998400-55000400 Enhancers Hela-S3 cervix
14 chr2:54998400-55000600 Enhancers Adipose Derived Mesenchymal Stem Cell Cultured Cells ES cell derived
15 chr2:54999200-55000200 Enhancers NHLF lung
16 chr2:54999200-55000600 Enhancers Stomach Mucosa stomach
17 chr2:54999800-55000200 Enhancers Bone Marrow Derived Cultured Mesenchymal Stem Cells Bone marrow
18 chr2:54999800-55000200 Flanking Active TSS NHEK skin
19 chr2:54999800-55000600 Enhancers Gastric stomach
20 chr2:55000000-55000200 Flanking Active TSS NH-A brain

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