Variant report

Variant rs74017952
Chromosome Location chr16:48431050-48431051
allele A/G
Outlinks Ensembl   UCSC
Chromatin state (count:14 , 50 per page) page: 1
No. Chromosome Location Chromatin state Cell line Tissue
1 chr16:48425800-48433000 Enhancers Placenta Placenta
2 chr16:48426600-48431200 Weak transcription Fetal Intestine Large intestine
3 chr16:48428400-48431200 Weak transcription H1 BMP4 Derived Trophoblast Cultured Cells ES cell derived
4 chr16:48429400-48446000 Weak transcription iPS DF 19.11 Cell Line embryonic stem cell
5 chr16:48430800-48431200 Enhancers Duodenum Mucosa Duodenum
6 chr16:48430800-48432000 Enhancers HepG2 liver
7 chr16:48431000-48431400 Enhancers Foreskin Keratinocyte Primary Cells skin02 Skin
8 chr16:48431000-48431400 Enhancers Liver Liver
9 chr16:48431000-48431400 Enhancers Stomach Mucosa stomach
10 chr16:48431000-48431400 Flanking Active TSS A549 lung
11 chr16:48431000-48431400 Enhancers HMEC breast
12 chr16:48431000-48431400 Enhancers NHEK skin
13 chr16:48431000-48432000 Enhancers Adipose Derived Mesenchymal Stem Cell Cultured Cells ES cell derived
14 chr16:48431000-48432200 Enhancers Foreskin Keratinocyte Primary Cells skin03 Skin

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