Variant report

Variant rs55721014
Chromosome Location chr5:41183779-41183780
allele A/G
Outlinks Ensembl   UCSC
Chromatin state (count:15 , 50 per page) page: 1
No. Chromosome Location Chromatin state Cell line Tissue
1 chr5:41173400-41184000 Weak transcription Pancreas Pancrea
2 chr5:41178000-41183800 Weak transcription IMR90 fetal lung fibroblasts Cell Line lung
3 chr5:41181400-41185200 Enhancers Fetal Intestine Small intestine
4 chr5:41181600-41184200 Enhancers Adipose Nuclei Adipose
5 chr5:41181600-41185200 Enhancers Fetal Intestine Large intestine
6 chr5:41181800-41184200 Enhancers HepG2 liver
7 chr5:41181800-41186400 Enhancers Stomach Mucosa stomach
8 chr5:41182000-41185000 Genic enhancers Liver Liver
9 chr5:41182000-41185600 Enhancers Mesenchymal Stem Cell Derived Adipocyte Cultured Cells ES cell derived
10 chr5:41182600-41184000 Enhancers Rectal Mucosa Donor 31 rectum
11 chr5:41182600-41184000 Weak transcription Small Intestine intestine
12 chr5:41182800-41184000 Enhancers Bone Marrow Derived Cultured Mesenchymal Stem Cells Bone marrow
13 chr5:41183400-41192200 Weak transcription Pancreatic Islets Pancreatic Islet
14 chr5:41183600-41184000 Enhancers Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells embryonic stem cell
15 chr5:41183600-41184200 Enhancers Ovary ovary

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