Variant report

Variant rs77033730
Chromosome Location chr2:55988891-55988892
allele G/T
Outlinks Ensembl   UCSC
Chromatin state (count:20 , 50 per page) page: 1
No. Chromosome Location Chromatin state Cell line Tissue
1 chr2:55985400-55991200 Enhancers HMEC breast
2 chr2:55986200-55989600 Enhancers NHEK skin
3 chr2:55986400-55989600 Enhancers Foreskin Keratinocyte Primary Cells skin03 Skin
4 chr2:55986600-55990000 Enhancers Breast variant Human Mammary Epithelial Cells (vHMEC) Breast
5 chr2:55987400-55991400 Enhancers Breast Myoepithelial Primary Cells Breast
6 chr2:55987800-55989400 Enhancers Adipose Nuclei Adipose
7 chr2:55987800-55990200 Enhancers HSMM muscle
8 chr2:55988000-55989600 Enhancers IMR90 fetal lung fibroblasts Cell Line lung
9 chr2:55988200-55989600 Enhancers Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells embryonic stem cell
10 chr2:55988200-55990000 Enhancers Foreskin Keratinocyte Primary Cells skin02 Skin
11 chr2:55988400-55989200 Flanking Active TSS Bone Marrow Derived Cultured Mesenchymal Stem Cells Bone marrow
12 chr2:55988600-55989000 Flanking Active TSS HSMMtube muscle
13 chr2:55988600-55989400 Enhancers Foreskin Melanocyte Primary Cells skin03 Skin
14 chr2:55988600-55989400 Enhancers Osteobl bone
15 chr2:55988600-55989600 Enhancers Stomach Smooth Muscle stomach
16 chr2:55988600-55991400 Enhancers Mesenchymal Stem Cell Derived Adipocyte Cultured Cells ES cell derived
17 chr2:55988800-55989200 Flanking Active TSS Muscle Satellite Cultured Cells --
18 chr2:55988800-55989200 Weak transcription Aorta Aorta
19 chr2:55988800-55989400 Enhancers Ovary ovary
20 chr2:55988800-55993000 Weak transcription HUVEC blood vessel

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