Variant report

Variant rs577945849
Chromosome Location chr14:105508770-105508771
allele A/G
Outlinks Ensembl   UCSC
Chromatin state (count:11 , 50 per page) page: 1
No. Chromosome Location Chromatin state Cell line Tissue
1 chr14:105500600-105512000 Weak transcription Foreskin Melanocyte Primary Cells skin01 Skin
2 chr14:105504800-105512000 Weak transcription Foreskin Melanocyte Primary Cells skin03 Skin
3 chr14:105507000-105509600 Weak transcription H1 Derived Mesenchymal Stem Cells ES cell derived
4 chr14:105507600-105508800 Enhancers A549 lung
5 chr14:105508000-105509600 Enhancers Fetal Heart heart
6 chr14:105508000-105509800 Enhancers Esophagus oesophagus
7 chr14:105508200-105508800 Bivalent Enhancer Foreskin Fibroblast Primary Cells skin01 Skin
8 chr14:105508200-105508800 Weak transcription Foreskin Keratinocyte Primary Cells skin02 Skin
9 chr14:105508400-105509000 Enhancers iPS DF 19.11 Cell Line embryonic stem cell
10 chr14:105508600-105508800 Bivalent Enhancer Adipose Derived Mesenchymal Stem Cell Cultured Cells ES cell derived
11 chr14:105508600-105508800 Bivalent Enhancer Foreskin Fibroblast Primary Cells skin02 Skin

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