Variant report

Variant rs10169169
Chromosome Location chr2:191412889-191412890
allele G/T
Outlinks Ensembl   UCSC
Chromatin state (count:14 , 50 per page) page: 1
No. Chromosome Location Chromatin state Cell line Tissue
1 chr2:191403000-191416800 Weak transcription Gastric stomach
2 chr2:191405400-191416800 Weak transcription Esophagus oesophagus
3 chr2:191409400-191413600 Enhancers Breast variant Human Mammary Epithelial Cells (vHMEC) Breast
4 chr2:191410400-191414000 Weak transcription NHLF lung
5 chr2:191410800-191418200 Weak transcription Pancreatic Islets Pancreatic Islet
6 chr2:191411000-191443000 Weak transcription Right Atrium heart
7 chr2:191411400-191413800 Enhancers HMEC breast
8 chr2:191411600-191413200 Enhancers Foreskin Keratinocyte Primary Cells skin02 Skin
9 chr2:191411600-191413800 Enhancers Foreskin Keratinocyte Primary Cells skin03 Skin
10 chr2:191411800-191416800 Weak transcription Psoas Muscle Psoas
11 chr2:191412000-191413600 Enhancers NHEK skin
12 chr2:191412000-191416600 Weak transcription HepG2 liver
13 chr2:191412600-191413000 Enhancers Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells embryonic stem cell
14 chr2:191412800-191413000 Enhancers Breast Myoepithelial Primary Cells Breast

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