Variant report

Variant rs73425799
Chromosome Location chr11:4513972-4513973
allele A/G
Outlinks Ensembl   UCSC
Chromatin state (count:9 , 50 per page) page: 1
No. Chromosome Location Chromatin state Cell line Tissue
1 chr11:4504200-4514000 Weak transcription Primary neutrophils fromperipheralblood blood
2 chr11:4513600-4514000 Enhancers Foreskin Fibroblast Primary Cells skin01 Skin
3 chr11:4513600-4514200 Enhancers Adipose Derived Mesenchymal Stem Cell Cultured Cells ES cell derived
4 chr11:4513600-4514200 Enhancers Monocytes-CD14+_RO01746 blood
5 chr11:4513600-4514400 Enhancers Placenta Amnion Placenta Amnion
6 chr11:4513600-4514400 Enhancers NHDF-Ad bronchial
7 chr11:4513600-4514600 Enhancers Fetal Intestine Small intestine
8 chr11:4513800-4514200 Enhancers Primary monocytes fromperipheralblood blood
9 chr11:4513800-4514200 Enhancers Fetal Intestine Large intestine

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