Variant report

Variant rs74172479
Chromosome Location chr19:45074764-45074765
allele A/G
Outlinks Ensembl   UCSC
Chromatin state (count:14 , 50 per page) page: 1
No. Chromosome Location Chromatin state Cell line Tissue
1 chr19:45070400-45080400 Weak transcription ES-I3 Cell Line embryonic stem cell
2 chr19:45070600-45075200 Weak transcription Primary monocytes fromperipheralblood blood
3 chr19:45073800-45076400 Enhancers K562 blood
4 chr19:45074200-45075600 Enhancers A549 lung
5 chr19:45074200-45076000 Flanking Active TSS HepG2 liver
6 chr19:45074400-45074800 Flanking Active TSS Liver Liver
7 chr19:45074400-45074800 Flanking Active TSS Fetal Intestine Small intestine
8 chr19:45074400-45075000 Bivalent Enhancer Stomach Mucosa stomach
9 chr19:45074400-45075200 Flanking Active TSS Duodenum Mucosa Duodenum
10 chr19:45074400-45075600 Enhancers H1 Derived Mesenchymal Stem Cells ES cell derived
11 chr19:45074400-45075600 Enhancers IMR90 fetal lung fibroblasts Cell Line lung
12 chr19:45074400-45077800 Enhancers Fetal Adrenal Gland Adrenal Gland
13 chr19:45074400-45078200 Enhancers Fetal Intestine Large intestine
14 chr19:45074600-45075000 Enhancers Fetal Kidney kidney

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