Variant report

Variant rs579568
Chromosome Location chr5:178804029-178804030
allele C/T
Outlinks Ensembl   UCSC
Chromatin state (count:17 , 50 per page) page: 1
No. Chromosome Location Chromatin state Cell line Tissue
1 chr5:178802400-178804600 Enhancers Ovary ovary
2 chr5:178802600-178804200 Weak transcription Foreskin Fibroblast Primary Cells skin01 Skin
3 chr5:178802600-178804800 Weak transcription Spleen Spleen
4 chr5:178803800-178804200 Enhancers Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells embryonic stem cell
5 chr5:178803800-178804400 Enhancers HSMM muscle
6 chr5:178803800-178804600 Enhancers Foreskin Fibroblast Primary Cells skin02 Skin
7 chr5:178803800-178804800 Enhancers Breast Myoepithelial Primary Cells Breast
8 chr5:178803800-178805000 Enhancers iPS DF 19.11 Cell Line embryonic stem cell
9 chr5:178803800-178805600 Enhancers IMR90 fetal lung fibroblasts Cell Line lung
10 chr5:178804000-178804200 Enhancers Mesenchymal Stem Cell Derived Adipocyte Cultured Cells ES cell derived
11 chr5:178804000-178804200 Enhancers HSMMtube muscle
12 chr5:178804000-178805600 Enhancers Muscle Satellite Cultured Cells --
13 chr5:178804000-178805600 Flanking Active TSS Osteobl bone
14 chr5:178804000-178806000 Flanking Active TSS Bone Marrow Derived Cultured Mesenchymal Stem Cells Bone marrow
15 chr5:178804000-178806400 Enhancers Fetal Muscle Leg muscle
16 chr5:178804000-178806800 Enhancers hESC Derived CD56+ Mesoderm Cultured Cells ES cell derived
17 chr5:178804000-178807400 Enhancers NHDF-Ad bronchial

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