Variant report

Variant rs17078698
Chromosome Location chr3:46241896-46241897
allele C/T
Outlinks Ensembl   UCSC
Chromatin state (count:15 , 50 per page) page: 1
No. Chromosome Location Chromatin state Cell line Tissue
1 chr3:46235400-46247600 Weak transcription Placenta Placenta
2 chr3:46235400-46249600 Weak transcription Breast variant Human Mammary Epithelial Cells (vHMEC) Breast
3 chr3:46239600-46243800 Weak transcription Adipose Derived Mesenchymal Stem Cell Cultured Cells ES cell derived
4 chr3:46239800-46249400 Weak transcription Primary T cells from cord blood blood
5 chr3:46240400-46242800 Weak transcription Primary mononuclear cells fromperipheralblood Blood
6 chr3:46241000-46244600 Weak transcription Spleen Spleen
7 chr3:46241200-46242200 Enhancers Brain Cingulate Gyrus brain
8 chr3:46241200-46242600 Strong transcription Primary Natural Killer cells fromperipheralblood blood
9 chr3:46241200-46246600 Genic enhancers Primary monocytes fromperipheralblood blood
10 chr3:46241400-46242400 Enhancers Brain Hippocampus Middle brain
11 chr3:46241600-46242400 Strong transcription Monocytes-CD14+_RO01746 blood
12 chr3:46241600-46247400 Weak transcription Brain Substantia Nigra brain
13 chr3:46241800-46242200 Enhancers Foreskin Melanocyte Primary Cells skin03 Skin
14 chr3:46241800-46242200 Enhancers Brain Anterior Caudate brain
15 chr3:46241800-46242800 Enhancers Primary neutrophils fromperipheralblood blood

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