Variant report

Variant rs67352743
Chromosome Location chr1:146548970-146548971
allele A/G
Outlinks Ensembl   UCSC
Chromatin state (count:14 , 50 per page) page: 1
No. Chromosome Location Chromatin state Cell line Tissue
1 chr1:146547800-146550000 Enhancers Liver Liver
2 chr1:146548200-146549600 ZNF genes & repeats Primary hematopoietic stem cells G-CSF-mobilized Male --
3 chr1:146548400-146549000 Bivalent/Poised TSS iPS-15b Cell Line embryonic stem cell
4 chr1:146548600-146551400 Bivalent Enhancer Foreskin Melanocyte Primary Cells skin03 Skin
5 chr1:146548800-146549000 Bivalent/Poised TSS H1 Cell Line embryonic stem cell
6 chr1:146548800-146549000 Flanking Bivalent TSS/Enh iPS DF 19.11 Cell Line embryonic stem cell
7 chr1:146548800-146549000 Flanking Bivalent TSS/Enh Foreskin Keratinocyte Primary Cells skin03 Skin
8 chr1:146548800-146549000 Bivalent Enhancer Brain Hippocampus Middle brain
9 chr1:146548800-146549000 Bivalent Enhancer Esophagus oesophagus
10 chr1:146548800-146551000 Bivalent Enhancer Right Ventricle heart
11 chr1:146548800-146551200 Bivalent Enhancer Breast Myoepithelial Primary Cells Breast
12 chr1:146548800-146551400 Bivalent Enhancer Foreskin Melanocyte Primary Cells skin01 Skin
13 chr1:146548800-146551400 Bivalent Enhancer Fetal Adrenal Gland Adrenal Gland
14 chr1:146548800-146552600 Bivalent Enhancer Fetal Muscle Trunk muscle

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