Variant report

Variant rs12487248
Chromosome Location chr3:17697696-17697697
allele C/T
Outlinks Ensembl   UCSC
Chromatin state (count:14 , 50 per page) page: 1
No. Chromosome Location Chromatin state Cell line Tissue
1 chr3:17668800-17706200 Weak transcription Primary B cells from cord blood blood
2 chr3:17681800-17714400 Weak transcription Breast variant Human Mammary Epithelial Cells (vHMEC) Breast
3 chr3:17689200-17704000 Weak transcription Primary B cells from peripheral blood blood
4 chr3:17694400-17721800 Weak transcription A549 lung
5 chr3:17695000-17706200 Weak transcription Primary hematopoietic stem cells short term culture blood
6 chr3:17697400-17697800 Enhancers Brain Hippocampus Middle brain
7 chr3:17697400-17697800 Flanking Active TSS GM12878-XiMat blood
8 chr3:17697400-17698600 Enhancers Primary hematopoietic stem cells G-CSF-mobilized Female --
9 chr3:17697600-17697800 Enhancers Brain Cingulate Gyrus brain
10 chr3:17697600-17697800 Enhancers Left Ventricle heart
11 chr3:17697600-17698000 Enhancers H9 Cell Line embryonic stem cell
12 chr3:17697600-17698000 Enhancers Brain Substantia Nigra brain
13 chr3:17697600-17698200 Enhancers Primary hematopoietic stem cells G-CSF-mobilized Male --
14 chr3:17697600-17707000 Weak transcription Sigmoid Colon Sigmoid Colon

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