Variant report

Variant rs7591608
Chromosome Location chr2:72571891-72571892
allele C/G
Outlinks Ensembl   UCSC
Chromatin state (count:12 , 50 per page) page: 1
No. Chromosome Location Chromatin state Cell line Tissue
1 chr2:72531200-72594800 Weak transcription Esophagus oesophagus
2 chr2:72553600-72576000 Weak transcription Fetal Heart heart
3 chr2:72553800-72594600 Weak transcription Aorta Aorta
4 chr2:72559200-72607400 Weak transcription Liver Liver
5 chr2:72560600-72594800 Weak transcription Pancreas Pancrea
6 chr2:72569000-72577600 Weak transcription Foreskin Keratinocyte Primary Cells skin02 Skin
7 chr2:72569000-72577800 Weak transcription Breast variant Human Mammary Epithelial Cells (vHMEC) Breast
8 chr2:72569600-72577600 Weak transcription Foreskin Keratinocyte Primary Cells skin03 Skin
9 chr2:72570800-72573600 ZNF genes & repeats hESC Derived CD184+ Endoderm Cultured Cells ES cell derived
10 chr2:72571800-72572000 ZNF genes & repeats hESC Derived CD56+ Mesoderm Cultured Cells ES cell derived
11 chr2:72571800-72572200 ZNF genes & repeats Adipose Nuclei Adipose
12 chr2:72571800-72572800 ZNF genes & repeats Breast Myoepithelial Primary Cells Breast

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