Variant report

Variant rs562254806
Chromosome Location chr9:100521803-100521804
allele A/G
Outlinks Ensembl   UCSC
Chromatin state (count:12 , 50 per page) page: 1
No. Chromosome Location Chromatin state Cell line Tissue
1 chr9:100515200-100524200 Weak transcription Esophagus oesophagus
2 chr9:100519400-100523600 Enhancers Fetal Intestine Large intestine
3 chr9:100519800-100523600 Enhancers Fetal Intestine Small intestine
4 chr9:100521000-100524600 Enhancers Adipose Nuclei Adipose
5 chr9:100521400-100523800 Enhancers Bone Marrow Derived Cultured Mesenchymal Stem Cells Bone marrow
6 chr9:100521400-100524000 Enhancers Liver Liver
7 chr9:100521600-100522200 Enhancers Colon Smooth Muscle Colon
8 chr9:100521600-100522200 Enhancers HSMMtube muscle
9 chr9:100521600-100523800 Enhancers Mesenchymal Stem Cell Derived Adipocyte Cultured Cells ES cell derived
10 chr9:100521800-100522800 Bivalent Enhancer Adipose Derived Mesenchymal Stem Cell Cultured Cells ES cell derived
11 chr9:100521800-100522800 Enhancers A549 lung
12 chr9:100521800-100522800 Flanking Active TSS HepG2 liver

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