Variant report

Variant rs10844819
Chromosome Location chr12:34261389-34261390
allele G/T
Outlinks Ensembl   UCSC
Chromatin state (count:14 , 50 per page) page: 1
No. Chromosome Location Chromatin state Cell line Tissue
1 chr12:34258400-34263200 ZNF genes & repeats ES-UCSF4 Cell Line embryonic stem cell
2 chr12:34258600-34262800 ZNF genes & repeats iPS DF 19.11 Cell Line embryonic stem cell
3 chr12:34259800-34262800 ZNF genes & repeats Foreskin Keratinocyte Primary Cells skin02 Skin
4 chr12:34260600-34262000 ZNF genes & repeats Foreskin Fibroblast Primary Cells skin01 Skin
5 chr12:34260800-34261400 Bivalent Enhancer Foreskin Melanocyte Primary Cells skin01 Skin
6 chr12:34260800-34261400 Flanking Bivalent TSS/Enh Adipose Nuclei Adipose
7 chr12:34261000-34261400 Flanking Bivalent TSS/Enh Foreskin Melanocyte Primary Cells skin03 Skin
8 chr12:34261000-34261400 Flanking Active TSS Pancreas Pancrea
9 chr12:34261000-34261400 Active TSS Right Atrium heart
10 chr12:34261200-34261400 Flanking Bivalent TSS/Enh Breast Myoepithelial Primary Cells Breast
11 chr12:34261200-34261400 Bivalent Enhancer Primary hematopoietic stem cells G-CSF-mobilized Female --
12 chr12:34261200-34261400 Bivalent Enhancer Right Ventricle heart
13 chr12:34261200-34261400 Bivalent/Poised TSS Stomach Smooth Muscle stomach
14 chr12:34261200-34264600 Enhancers Placenta Placenta

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