Variant report

Variant rs4958536
Chromosome Location chr5:151785054-151785055
allele A/G
Outlinks Ensembl   UCSC
Chromatin state (count:16 , 50 per page) page: 1
No. Chromosome Location Chromatin state Cell line Tissue
1 chr5:151782800-151790800 Weak transcription Brain Anterior Caudate brain
2 chr5:151784400-151785400 Enhancers Fetal Muscle Trunk muscle
3 chr5:151784600-151785200 Enhancers hESC Derived CD184+ Endoderm Cultured Cells ES cell derived
4 chr5:151784600-151785400 Active TSS Foreskin Keratinocyte Primary Cells skin03 Skin
5 chr5:151784600-151785400 Active TSS Pancreatic Islets Pancreatic Islet
6 chr5:151784800-151785200 Active TSS ES-I3 Cell Line embryonic stem cell
7 chr5:151784800-151785200 Flanking Active TSS Foreskin Keratinocyte Primary Cells skin02 Skin
8 chr5:151784800-151785200 Enhancers Adipose Nuclei Adipose
9 chr5:151784800-151785200 Enhancers Brain Hippocampus Middle brain
10 chr5:151784800-151785200 Enhancers Duodenum Mucosa Duodenum
11 chr5:151784800-151785200 Active TSS Fetal Intestine Large intestine
12 chr5:151784800-151785200 Flanking Active TSS Fetal Lung lung
13 chr5:151784800-151785200 Active TSS NHEK skin
14 chr5:151785000-151785400 Enhancers HUES6 Cell Line embryonic stem cell
15 chr5:151785000-151785400 Bivalent Enhancer iPS-15b Cell Line embryonic stem cell
16 chr5:151785000-151785400 Enhancers iPS-20b Cell Line embryonic stem cell

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