Variant report

Variant rs10203965
Chromosome Location chr2:72576344-72576345
allele C/G
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 chr2:72553800-72594600 Weak transcription Aorta Aorta
3 chr2:72559200-72607400 Weak transcription Liver Liver
4 chr2:72560600-72594800 Weak transcription Pancreas Pancrea
5 chr2:72569000-72577600 Weak transcription Foreskin Keratinocyte Primary Cells skin02 Skin
6 chr2:72569000-72577800 Weak transcription Breast variant Human Mammary Epithelial Cells (vHMEC) Breast
7 chr2:72569600-72577600 Weak transcription Foreskin Keratinocyte Primary Cells skin03 Skin
8 chr2:72572200-72601400 Weak transcription Adipose Nuclei Adipose
9 chr2:72572200-72607200 Weak transcription Psoas Muscle Psoas
10 chr2:72573600-72578000 Weak transcription hESC Derived CD184+ Endoderm Cultured Cells ES cell derived
11 chr2:72573600-72595000 Weak transcription Breast Myoepithelial Primary Cells Breast
12 chr2:72574200-72594800 Weak transcription Placenta Placenta
13 chr2:72575200-72588800 Weak transcription H1 Derived Mesenchymal Stem Cells ES cell derived
14 chr2:72576000-72576600 Enhancers Fetal Heart heart
15 chr2:72576000-72576800 Enhancers HUVEC blood vessel
16 chr2:72576200-72576400 Enhancers HUES48 Cell Line embryonic stem cell

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