Variant report

Variant rs189869522
Chromosome Location chr10:5133598-5133599
allele C/T
Outlinks Ensembl   UCSC
Chromatin state (count:10 , 50 per page) page: 1
No. Chromosome Location Chromatin state Cell line Tissue
1 chr10:5131800-5133600 Enhancers NHEK skin
2 chr10:5132200-5133600 Enhancers HMEC breast
3 chr10:5132200-5136200 Enhancers Breast variant Human Mammary Epithelial Cells (vHMEC) Breast
4 chr10:5132400-5135800 Enhancers Foreskin Keratinocyte Primary Cells skin03 Skin
5 chr10:5132400-5136000 Weak transcription Duodenum Mucosa Duodenum
6 chr10:5132600-5134600 Weak transcription Stomach Mucosa stomach
7 chr10:5132800-5135600 Weak transcription HepG2 liver
8 chr10:5133400-5133600 Enhancers Mesenchymal Stem Cell Derived Adipocyte Cultured Cells ES cell derived
9 chr10:5133400-5134200 Weak transcription A549 lung
10 chr10:5133400-5136200 Weak transcription Adipose Nuclei Adipose

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