Variant report

Variant rs58582296
Chromosome Location chr2:72568147-72568148
allele C/T
Outlinks Ensembl   UCSC
Chromatin state (count:16 , 50 per page) page: 1
No. Chromosome Location Chromatin state Cell line Tissue
1 chr2:72531200-72594800 Weak transcription Esophagus oesophagus
2 chr2:72552600-72568600 Weak transcription Fetal Brain Male brain
3 chr2:72553600-72576000 Weak transcription Fetal Heart heart
4 chr2:72553800-72594600 Weak transcription Aorta Aorta
5 chr2:72558000-72568800 Weak transcription HMEC breast
6 chr2:72559200-72607400 Weak transcription Liver Liver
7 chr2:72560600-72594800 Weak transcription Pancreas Pancrea
8 chr2:72561600-72571800 Weak transcription Adipose Nuclei Adipose
9 chr2:72567600-72568200 Enhancers Adipose Derived Mesenchymal Stem Cell Cultured Cells ES cell derived
10 chr2:72567600-72568200 Enhancers NHDF-Ad bronchial
11 chr2:72567600-72569000 Enhancers Foreskin Keratinocyte Primary Cells skin02 Skin
12 chr2:72567600-72569800 Enhancers NHEK skin
13 chr2:72567800-72568200 Enhancers Psoas Muscle Psoas
14 chr2:72567800-72569000 Enhancers Breast variant Human Mammary Epithelial Cells (vHMEC) Breast
15 chr2:72567800-72569600 Enhancers Foreskin Keratinocyte Primary Cells skin03 Skin
16 chr2:72568000-72568200 Enhancers H1 BMP4 Derived Mesendoderm Cultured Cells ES cell derived

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