Variant report

Variant rs3101761
Chromosome Location chr5:167503643-167503644
allele C/G
Outlinks Ensembl   UCSC
Chromatin state (count:16 , 50 per page) page: 1
No. Chromosome Location Chromatin state Cell line Tissue
1 chr5:167491800-167509200 Weak transcription H9 Derived Neuron Cultured Cells ES cell derived
2 chr5:167497800-167504400 Strong transcription Foreskin Keratinocyte Primary Cells skin02 Skin
3 chr5:167500600-167504800 Weak transcription Breast Myoepithelial Primary Cells Breast
4 chr5:167501000-167512800 Weak transcription Placenta Amnion Placenta Amnion
5 chr5:167501600-167514800 Weak transcription NHEK skin
6 chr5:167501800-167503800 Weak transcription Left Ventricle heart
7 chr5:167501800-167504400 Enhancers Primary hematopoietic stem cells G-CSF-mobilized Female --
8 chr5:167501800-167511800 Weak transcription H1 Derived Mesenchymal Stem Cells ES cell derived
9 chr5:167502000-167504400 Enhancers Primary hematopoietic stem cells G-CSF-mobilized Male --
10 chr5:167502200-167503800 Weak transcription Primary hematopoietic stem cells blood
11 chr5:167502600-167503800 Weak transcription Primary hematopoietic stem cells short term culture blood
12 chr5:167503400-167504400 Enhancers Mesenchymal Stem Cell Derived Adipocyte Cultured Cells ES cell derived
13 chr5:167503400-167504400 Strong transcription Foreskin Keratinocyte Primary Cells skin03 Skin
14 chr5:167503600-167503800 Enhancers Right Ventricle heart
15 chr5:167503600-167504000 Enhancers ES-UCSF4 Cell Line embryonic stem cell
16 chr5:167503600-167504200 Enhancers Brain Hippocampus Middle brain

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