Variant report

Variant rs634686
Chromosome Location chr6:150691456-150691457
allele A/G
Outlinks Ensembl   UCSC
Chromatin state (count:16 , 50 per page) page: 1
No. Chromosome Location Chromatin state Cell line Tissue
1 chr6:150689200-150693200 Enhancers Fetal Intestine Large intestine
2 chr6:150689200-150693400 Enhancers Fetal Intestine Small intestine
3 chr6:150689800-150691800 Flanking Active TSS Liver Liver
4 chr6:150690000-150691600 Active TSS Rectal Mucosa Donor 29 rectum
5 chr6:150690200-150691600 Active TSS Colonic Mucosa Colon
6 chr6:150691000-150691600 Active TSS Fetal Kidney kidney
7 chr6:150691000-150698200 Weak transcription Stomach Mucosa stomach
8 chr6:150691200-150691600 Flanking Active TSS Duodenum Mucosa Duodenum
9 chr6:150691200-150691600 ZNF genes & repeats Lung lung
10 chr6:150691400-150691600 Bivalent Enhancer H1 BMP4 Derived Trophoblast Cultured Cells ES cell derived
11 chr6:150691400-150691600 Flanking Bivalent TSS/Enh H1 Derived Mesenchymal Stem Cells ES cell derived
12 chr6:150691400-150691600 Enhancers H1 Derived Neuronal Progenitor Cultured Cells ES cell derived
13 chr6:150691400-150691600 Enhancers iPS DF 19.11 Cell Line embryonic stem cell
14 chr6:150691400-150691600 Enhancers Fetal Lung lung
15 chr6:150691400-150691600 Flanking Active TSS Gastric stomach
16 chr6:150691400-150691600 Enhancers Pancreas Pancrea

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