Variant report

Variant rs4971711
Chromosome Location chr2:51184730-51184731
allele C/T
Outlinks Ensembl   UCSC
Chromatin state (count:16 , 50 per page) page: 1
No. Chromosome Location Chromatin state Cell line Tissue
1 chr2:51176400-51190600 Weak transcription iPS-15b Cell Line embryonic stem cell
2 chr2:51179800-51186000 Enhancers Breast Myoepithelial Primary Cells Breast
3 chr2:51180400-51189400 Weak transcription ES-I3 Cell Line embryonic stem cell
4 chr2:51182200-51185200 Weak transcription Fetal Muscle Leg muscle
5 chr2:51183000-51185200 Weak transcription Cortex derived primary cultured neurospheres brain
6 chr2:51183200-51190000 Weak transcription Ganglion Eminence derived primary cultured neurospheres brain
7 chr2:51183400-51185200 Weak transcription Pancreatic Islets Pancreatic Islet
8 chr2:51183800-51185000 Enhancers Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells embryonic stem cell
9 chr2:51183800-51185200 Weak transcription Brain Cingulate Gyrus brain
10 chr2:51184000-51185400 Enhancers Breast variant Human Mammary Epithelial Cells (vHMEC) Breast
11 chr2:51184000-51185400 Enhancers HMEC breast
12 chr2:51184200-51185400 Enhancers Brain Hippocampus Middle brain
13 chr2:51184400-51185000 Enhancers Bone Marrow Derived Cultured Mesenchymal Stem Cells Bone marrow
14 chr2:51184600-51184800 Active TSS Mesenchymal Stem Cell Derived Adipocyte Cultured Cells ES cell derived
15 chr2:51184600-51185400 Enhancers Brain Anterior Caudate brain
16 chr2:51184600-51185400 Enhancers Brain Germinal Matrix brain

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