Variant report

Variant rs10849549
Chromosome Location chr12:850288-850289
allele C/T
Outlinks Ensembl   UCSC
Chromatin state (count:11 , 50 per page) page: 1
No. Chromosome Location Chromatin state Cell line Tissue
1 chr12:847600-850400 Enhancers HepG2 liver
2 chr12:849600-850400 Enhancers Placenta Placenta
3 chr12:849600-850400 Enhancers Stomach Mucosa stomach
4 chr12:849600-850800 Enhancers H1 BMP4 Derived Mesendoderm Cultured Cells ES cell derived
5 chr12:849800-850600 Enhancers Foreskin Keratinocyte Primary Cells skin02 Skin
6 chr12:849800-850600 Enhancers Foreskin Keratinocyte Primary Cells skin03 Skin
7 chr12:849800-850800 Enhancers Fetal Heart heart
8 chr12:849800-850800 Enhancers NHEK skin
9 chr12:850000-850400 Enhancers HMEC breast
10 chr12:850000-850800 Enhancers hESC Derived CD184+ Endoderm Cultured Cells ES cell derived
11 chr12:850200-850400 Enhancers Primary T regulatory cells fromperipheralblood blood

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