Variant report

Variant rs4970862
Chromosome Location chr1:145421477-145421478
allele C/T
Outlinks Ensembl   UCSC
Chromatin state (count:20 , 50 per page) page: 1
No. Chromosome Location Chromatin state Cell line Tissue
1 chr1:145415800-145423400 Weak transcription Lung lung
2 chr1:145415800-145434600 Weak transcription Right Atrium heart
3 chr1:145417200-145421600 Weak transcription Skeletal Muscle Male skeletal muscle
4 chr1:145417600-145421600 Weak transcription Liver Liver
5 chr1:145418000-145427000 Weak transcription Skeletal Muscle Female skeletal muscle
6 chr1:145419000-145427000 Weak transcription Foreskin Fibroblast Primary Cells skin02 Skin
7 chr1:145421000-145421600 Enhancers Foreskin Fibroblast Primary Cells skin01 Skin
8 chr1:145421000-145421800 Enhancers Breast variant Human Mammary Epithelial Cells (vHMEC) Breast
9 chr1:145421000-145422000 Enhancers NH-A brain
10 chr1:145421000-145422200 Enhancers Adipose Derived Mesenchymal Stem Cell Cultured Cells ES cell derived
11 chr1:145421200-145421800 Enhancers HSMM muscle
12 chr1:145421200-145421800 Enhancers HSMMtube muscle
13 chr1:145421200-145422000 Enhancers K562 blood
14 chr1:145421200-145422200 Enhancers NHDF-Ad bronchial
15 chr1:145421400-145421600 Enhancers Breast Myoepithelial Primary Cells Breast
16 chr1:145421400-145421800 Enhancers Bone Marrow Derived Cultured Mesenchymal Stem Cells Bone marrow
17 chr1:145421400-145421800 Enhancers Primary T helper 17 cells PMA-I stimulated --
18 chr1:145421400-145421800 Enhancers NHEK skin
19 chr1:145421400-145421800 Enhancers Osteobl bone
20 chr1:145421400-145422200 Enhancers Muscle Satellite Cultured Cells --

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