Variant report

Variant rs181705828
Chromosome Location chr2:56750569-56750570
allele A/T
Outlinks Ensembl   UCSC
Chromatin state (count:17 , 50 per page) page: 1
No. Chromosome Location Chromatin state Cell line Tissue
1 chr2:56748800-56752600 Enhancers Fetal Heart heart
2 chr2:56749600-56750600 Enhancers Liver Liver
3 chr2:56749600-56751800 Enhancers HSMM muscle
4 chr2:56749800-56750600 Enhancers Foreskin Keratinocyte Primary Cells skin03 Skin
5 chr2:56749800-56750600 Enhancers Fetal Stomach stomach
6 chr2:56749800-56750600 Enhancers Psoas Muscle Psoas
7 chr2:56749800-56750600 Enhancers HSMMtube muscle
8 chr2:56749800-56751400 Enhancers Bone Marrow Derived Cultured Mesenchymal Stem Cells Bone marrow
9 chr2:56749800-56751400 Enhancers Muscle Satellite Cultured Cells --
10 chr2:56750000-56750600 Enhancers NHEK skin
11 chr2:56750200-56750600 Enhancers Adipose Nuclei Adipose
12 chr2:56750200-56750800 Flanking Active TSS Mesenchymal Stem Cell Derived Adipocyte Cultured Cells ES cell derived
13 chr2:56750200-56751000 Active TSS Fetal Muscle Leg muscle
14 chr2:56750400-56750600 Enhancers Skeletal Muscle Male skeletal muscle
15 chr2:56750400-56750600 Active TSS Skeletal Muscle Female skeletal muscle
16 chr2:56750400-56750600 Enhancers A549 lung
17 chr2:56750400-56751400 Weak transcription Foreskin Keratinocyte Primary Cells skin02 Skin

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