Variant report

Variant rs67176648
Chromosome Location chr14:105506915-105506916
allele A/CG
Outlinks Ensembl   UCSC
Chromatin state (count:10 , 50 per page) page: 1
No. Chromosome Location Chromatin state Cell line Tissue
1 chr14:105497800-105507800 Weak transcription K562 blood
2 chr14:105500600-105508000 Weak transcription Foreskin Fibroblast Primary Cells skin02 Skin
3 chr14:105500600-105512000 Weak transcription Foreskin Melanocyte Primary Cells skin01 Skin
4 chr14:105500800-105507600 Weak transcription Foreskin Keratinocyte Primary Cells skin02 Skin
5 chr14:105504400-105507200 Weak transcription Mesenchymal Stem Cell Derived Adipocyte Cultured Cells ES cell derived
6 chr14:105504800-105512000 Weak transcription Foreskin Melanocyte Primary Cells skin03 Skin
7 chr14:105506200-105507000 Enhancers H1 Derived Mesenchymal Stem Cells ES cell derived
8 chr14:105506200-105507000 Enhancers HepG2 liver
9 chr14:105506200-105507600 Weak transcription A549 lung
10 chr14:105506800-105508000 Weak transcription Fetal Heart heart

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