Variant report

Variant rs17018278
Chromosome Location chr3:319314-319315
allele A/C/G/T
Outlinks Ensembl   UCSC
Chromatin state (count:16 , 50 per page) page: 1
No. Chromosome Location Chromatin state Cell line Tissue
1 chr3:314400-319600 Enhancers Primary B cells from peripheral blood blood
2 chr3:315800-320200 Enhancers Adipose Derived Mesenchymal Stem Cell Cultured Cells ES cell derived
3 chr3:315800-321800 Enhancers Foreskin Melanocyte Primary Cells skin03 Skin
4 chr3:317400-319600 Weak transcription Foreskin Melanocyte Primary Cells skin01 Skin
5 chr3:318200-319400 Enhancers Primary B cells from cord blood blood
6 chr3:318200-321800 Enhancers Fetal Brain Male brain
7 chr3:318800-320000 Enhancers Mesenchymal Stem Cell Derived Adipocyte Cultured Cells ES cell derived
8 chr3:319000-320000 Enhancers Primary hematopoietic stem cells G-CSF-mobilized Female --
9 chr3:319000-320400 Enhancers Fetal Kidney kidney
10 chr3:319000-320800 Enhancers Primary hematopoietic stem cells short term culture blood
11 chr3:319200-319400 Enhancers Brain Angular Gyrus brain
12 chr3:319200-320000 Enhancers Primary hematopoietic stem cells blood
13 chr3:319200-320600 Enhancers Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells embryonic stem cell
14 chr3:319200-320600 Flanking Active TSS GM12878-XiMat blood
15 chr3:319200-321400 Enhancers Ganglion Eminence derived primary cultured neurospheres brain
16 chr3:319200-321600 Enhancers Brain Anterior Caudate brain

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