Variant report

Variant rs1987522
Chromosome Location chr4:174267523-174267524
allele C/G
Outlinks Ensembl   UCSC
Chromatin state (count:22 , 50 per page) page: 1
No. Chromosome Location Chromatin state Cell line Tissue
1 chr4:174256800-174280400 Weak transcription Aorta Aorta
2 chr4:174259200-174290400 Weak transcription Thymus Thymus
3 chr4:174265200-174267600 Weak transcription HSMMtube muscle
4 chr4:174265400-174278200 Weak transcription Ovary ovary
5 chr4:174265600-174267600 Weak transcription ES-I3 Cell Line embryonic stem cell
6 chr4:174266200-174268800 Weak transcription ES-UCSF4 Cell Line embryonic stem cell
7 chr4:174266400-174268000 Enhancers Muscle Satellite Cultured Cells --
8 chr4:174266400-174268000 Enhancers NHDF-Ad bronchial
9 chr4:174266400-174268200 Enhancers HSMM muscle
10 chr4:174266800-174267600 Enhancers Breast variant Human Mammary Epithelial Cells (vHMEC) Breast
11 chr4:174266800-174267800 Enhancers Mesenchymal Stem Cell Derived Adipocyte Cultured Cells ES cell derived
12 chr4:174266800-174267800 Enhancers Adipose Derived Mesenchymal Stem Cell Cultured Cells ES cell derived
13 chr4:174266800-174267800 Enhancers Foreskin Keratinocyte Primary Cells skin02 Skin
14 chr4:174267000-174267600 Enhancers iPS-18 Cell Line embryonic stem cell
15 chr4:174267200-174267600 Active TSS Bone Marrow Derived Cultured Mesenchymal Stem Cells Bone marrow
16 chr4:174267200-174267600 Enhancers NHEK skin
17 chr4:174267200-174267600 Flanking Active TSS Osteobl bone
18 chr4:174267400-174267600 Enhancers iPS-20b Cell Line embryonic stem cell
19 chr4:174267400-174267800 Enhancers H1 Cell Line embryonic stem cell
20 chr4:174267400-174267800 Enhancers HUES48 Cell Line embryonic stem cell
21 chr4:174267400-174267800 Flanking Active TSS Foreskin Fibroblast Primary Cells skin01 Skin
22 chr4:174267400-174267800 Enhancers NH-A brain

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