Variant report

Variant rs1563743
Chromosome Location chr4:131399926-131399927
allele C/G
Outlinks Ensembl   UCSC
Chromatin state (count:11 , 50 per page) page: 1
No. Chromosome Location Chromatin state Cell line Tissue
1 chr4:131399000-131401000 Enhancers Mesenchymal Stem Cell Derived Adipocyte Cultured Cells ES cell derived
2 chr4:131399000-131401000 Enhancers Adipose Derived Mesenchymal Stem Cell Cultured Cells ES cell derived
3 chr4:131399400-131400000 Enhancers H1 BMP4 Derived Trophoblast Cultured Cells ES cell derived
4 chr4:131399400-131400000 Enhancers H9 Derived Neuron Cultured Cells ES cell derived
5 chr4:131399400-131400800 Enhancers IMR90 fetal lung fibroblasts Cell Line lung
6 chr4:131399400-131400800 Enhancers HMEC breast
7 chr4:131399600-131400000 Enhancers HUES6 Cell Line embryonic stem cell
8 chr4:131399600-131400000 Enhancers Foreskin Keratinocyte Primary Cells skin03 Skin
9 chr4:131399600-131400800 Enhancers Breast variant Human Mammary Epithelial Cells (vHMEC) Breast
10 chr4:131399800-131400200 Enhancers Muscle Satellite Cultured Cells --
11 chr4:131399800-131400600 Weak transcription NHLF lung

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