Variant report

Variant rs143259194
Chromosome Location chr14:105509680-105509681
allele A/G
Outlinks Ensembl   UCSC
Chromatin state (count:10 , 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 chr14:105508000-105509800 Enhancers Esophagus oesophagus
4 chr14:105509400-105509800 Enhancers Primary B cells from cord blood blood
5 chr14:105509400-105509800 Bivalent Enhancer Placenta Placenta
6 chr14:105509400-105511200 Enhancers Primary monocytes fromperipheralblood blood
7 chr14:105509600-105510000 Weak transcription Fetal Heart heart
8 chr14:105509600-105510200 ZNF genes & repeats H1 Derived Mesenchymal Stem Cells ES cell derived
9 chr14:105509600-105512000 Weak transcription Foreskin Keratinocyte Primary Cells skin02 Skin
10 chr14:105509600-105512800 Enhancers Monocytes-CD14+_RO01746 blood

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