Variant report

Variant rs6482626
Chromosome Location chr10:27702725-27702726
allele A/G
Outlinks Ensembl   UCSC
Chromatin state (count:14 , 50 per page) page: 1
No. Chromosome Location Chromatin state Cell line Tissue
1 chr10:27702200-27702800 Flanking Active TSS iPS DF 19.11 Cell Line embryonic stem cell
2 chr10:27702400-27702800 Bivalent Enhancer Foreskin Keratinocyte Primary Cells skin02 Skin
3 chr10:27702400-27702800 Flanking Active TSS Pancreas Pancrea
4 chr10:27702400-27703000 Bivalent/Poised TSS Primary hematopoietic stem cells G-CSF-mobilized Male --
5 chr10:27702400-27703000 Bivalent Enhancer Fetal Stomach stomach
6 chr10:27702400-27703200 Bivalent Enhancer Primary monocytes fromperipheralblood blood
7 chr10:27702400-27703400 Bivalent/Poised TSS Duodenum Smooth Muscle Duodenum
8 chr10:27702400-27703600 Active TSS Adipose Nuclei Adipose
9 chr10:27702600-27702800 ZNF genes & repeats Primary neutrophils fromperipheralblood blood
10 chr10:27702600-27702800 Bivalent/Poised TSS Foreskin Melanocyte Primary Cells skin03 Skin
11 chr10:27702600-27702800 Bivalent Enhancer Brain Germinal Matrix brain
12 chr10:27702600-27702800 Bivalent Enhancer Fetal Muscle Trunk muscle
13 chr10:27702600-27703200 Bivalent/Poised TSS Foreskin Keratinocyte Primary Cells skin03 Skin
14 chr10:27702600-27703400 Bivalent/Poised TSS Foreskin Melanocyte Primary Cells skin01 Skin

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