Variant report

Variant rs28616636
Chromosome Location chr14:66970091-66970092
allele A/G
Outlinks Ensembl   UCSC
Chromatin state (count:14 , 50 per page) page: 1
No. Chromosome Location Chromatin state Cell line Tissue
1 chr14:66952200-66973400 Weak transcription H9 Derived Neuron Cultured Cells ES cell derived
2 chr14:66954400-66970200 Weak transcription Gastric stomach
3 chr14:66962800-66973600 Weak transcription Primary hematopoietic stem cells blood
4 chr14:66962800-66974000 Weak transcription Aorta Aorta
5 chr14:66963000-66973600 Weak transcription Colon Smooth Muscle Colon
6 chr14:66963600-66973800 Weak transcription Primary T killer naive cells fromperipheralblood blood
7 chr14:66963800-66970200 Weak transcription Foreskin Keratinocyte Primary Cells skin03 Skin
8 chr14:66964400-66973400 Weak transcription GM12878-XiMat blood
9 chr14:66964600-66973200 Weak transcription Primary hematopoietic stem cells short term culture blood
10 chr14:66964600-66973200 Weak transcription Primary hematopoietic stem cells G-CSF-mobilized Female --
11 chr14:66965000-66973600 Weak transcription Primary T helper naive cells fromperipheralblood blood
12 chr14:66968600-66970800 Enhancers Liver Liver
13 chr14:66969400-66973000 Weak transcription HepG2 liver
14 chr14:66969800-66970800 Enhancers Breast Myoepithelial Primary Cells Breast

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