Variant report

Variant rs6658353
Chromosome Location chr1:161469054-161469055
allele C/G
Outlinks Ensembl   UCSC
Chromatin state (count:16 , 50 per page) page: 1
No. Chromosome Location Chromatin state Cell line Tissue
1 chr1:161466600-161471400 Enhancers Foreskin Melanocyte Primary Cells skin03 Skin
2 chr1:161467800-161471600 Enhancers Primary monocytes fromperipheralblood blood
3 chr1:161467800-161471600 Enhancers Primary hematopoietic stem cells short term culture blood
4 chr1:161468200-161469200 Enhancers Brain Anterior Caudate brain
5 chr1:161468400-161469200 Enhancers Brain Substantia Nigra brain
6 chr1:161468400-161469200 Enhancers Duodenum Mucosa Duodenum
7 chr1:161468600-161469400 Enhancers GM12878-XiMat blood
8 chr1:161468600-161469600 Weak transcription Foreskin Melanocyte Primary Cells skin01 Skin
9 chr1:161468600-161470200 Enhancers Primary hematopoietic stem cells blood
10 chr1:161468600-161472400 Enhancers K562 blood
11 chr1:161469000-161469200 Bivalent Enhancer Primary hematopoietic stem cells G-CSF-mobilized Female --
12 chr1:161469000-161469600 Enhancers Primary T helper memory cells from peripheral blood 2 blood
13 chr1:161469000-161469600 Enhancers Primary Natural Killer cells fromperipheralblood blood
14 chr1:161469000-161469800 Bivalent Enhancer Primary T helper memory cells from peripheral blood 1 blood
15 chr1:161469000-161469800 Flanking Active TSS Monocytes-CD14+_RO01746 blood
16 chr1:161469000-161470200 Flanking Active TSS Primary neutrophils fromperipheralblood blood

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