Variant report

Variant rs16842455
Chromosome Location chr3:100356385-100356386
allele A/G
Outlinks Ensembl   UCSC
Chromatin state (count:15 , 50 per page) page: 1
No. Chromosome Location Chromatin state Cell line Tissue
1 chr3:100354000-100357800 Weak transcription Fetal Brain Male brain
2 chr3:100354400-100356800 Weak transcription Pancreas Pancrea
3 chr3:100354400-100359000 Weak transcription Sigmoid Colon Sigmoid Colon
4 chr3:100354400-100360000 Weak transcription Rectal Mucosa Donor 31 rectum
5 chr3:100354600-100359600 Weak transcription Primary hematopoietic stem cells G-CSF-mobilized Male --
6 chr3:100354800-100357600 Genic enhancers Fetal Intestine Small intestine
7 chr3:100355000-100359800 Weak transcription Small Intestine intestine
8 chr3:100355200-100357000 Strong transcription Primary neutrophils fromperipheralblood blood
9 chr3:100355200-100359000 Weak transcription HepG2 liver
10 chr3:100355600-100357600 Strong transcription Duodenum Mucosa Duodenum
11 chr3:100355800-100356400 Flanking Active TSS Liver Liver
12 chr3:100355800-100356600 Enhancers Adipose Derived Mesenchymal Stem Cell Cultured Cells ES cell derived
13 chr3:100356000-100356600 Bivalent Enhancer NHDF-Ad bronchial
14 chr3:100356200-100356600 Bivalent Enhancer Osteobl bone
15 chr3:100356200-100359200 Genic enhancers Fetal Intestine Large intestine

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