Variant report

Variant rs62515736
Chromosome Location chr8:43101674-43101675
allele A/T
Outlinks Ensembl   UCSC
Chromatin state (count:15 , 50 per page) page: 1
No. Chromosome Location Chromatin state Cell line Tissue
1 chr8:43101400-43101800 Flanking Bivalent TSS/Enh Foreskin Fibroblast Primary Cells skin01 Skin
2 chr8:43101400-43101800 ZNF genes & repeats Foreskin Fibroblast Primary Cells skin02 Skin
3 chr8:43101400-43101800 Bivalent Enhancer HMEC breast
4 chr8:43101400-43102000 Flanking Bivalent TSS/Enh Foreskin Melanocyte Primary Cells skin01 Skin
5 chr8:43101400-43102200 Bivalent/Poised TSS Foreskin Keratinocyte Primary Cells skin02 Skin
6 chr8:43101400-43102200 Flanking Bivalent TSS/Enh Foreskin Keratinocyte Primary Cells skin03 Skin
7 chr8:43101400-43102400 ZNF genes & repeats H1 Cell Line embryonic stem cell
8 chr8:43101400-43102400 Bivalent Enhancer Placenta Placenta
9 chr8:43101400-43102400 Enhancers Gastric stomach
10 chr8:43101400-43102800 ZNF genes & repeats iPS DF 19.11 Cell Line embryonic stem cell
11 chr8:43101400-43102800 Flanking Bivalent TSS/Enh Foreskin Melanocyte Primary Cells skin03 Skin
12 chr8:43101400-43102800 Enhancers Pancreas Pancrea
13 chr8:43101600-43101800 Bivalent Enhancer Stomach Smooth Muscle stomach
14 chr8:43101600-43102200 Bivalent/Poised TSS HSMMtube muscle
15 chr8:43101600-43102400 Bivalent/Poised TSS Muscle Satellite Cultured Cells --

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