Variant report

Variant rs3758909
Chromosome Location chr11:108534970-108534971
allele A/G
Outlinks Ensembl   UCSC
Chromatin state (count:16 , 50 per page) page: 1
No. Chromosome Location Chromatin state Cell line Tissue
1 chr11:108532000-108535200 Weak transcription H9 Derived Neuronal Progenitor Cultured Cells ES cell derived
2 chr11:108532000-108535200 Weak transcription Foreskin Melanocyte Primary Cells skin03 Skin
3 chr11:108532200-108535000 Weak transcription H9 Derived Neuron Cultured Cells ES cell derived
4 chr11:108532200-108535200 Weak transcription Ganglion Eminence derived primary cultured neurospheres brain
5 chr11:108533600-108535200 Enhancers Primary B cells from peripheral blood blood
6 chr11:108534600-108535000 Enhancers HepG2 liver
7 chr11:108534600-108535200 Enhancers Primary monocytes fromperipheralblood blood
8 chr11:108534800-108535000 Enhancers Breast Myoepithelial Primary Cells Breast
9 chr11:108534800-108535000 Enhancers Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells embryonic stem cell
10 chr11:108534800-108535000 Enhancers Primary hematopoietic stem cells G-CSF-mobilized Male --
11 chr11:108534800-108535000 Enhancers Adipose Nuclei Adipose
12 chr11:108534800-108535000 Enhancers Brain Substantia Nigra brain
13 chr11:108534800-108535000 Enhancers Skeletal Muscle Female skeletal muscle
14 chr11:108534800-108535200 Enhancers Primary B cells from cord blood blood
15 chr11:108534800-108535200 Enhancers Primary T cells fromperipheralblood blood
16 chr11:108534800-108535200 Enhancers GM12878-XiMat blood

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