Variant report

Variant rs17069614
Chromosome Location chr5:167444001-167444002
allele C/G
Outlinks Ensembl   UCSC
Chromatin state (count:16 , 50 per page) page: 1
No. Chromosome Location Chromatin state Cell line Tissue
1 chr5:167423400-167455400 Weak transcription H1 Derived Mesenchymal Stem Cells ES cell derived
2 chr5:167434800-167447600 Weak transcription NH-A brain
3 chr5:167438000-167448200 Weak transcription Cortex derived primary cultured neurospheres brain
4 chr5:167441400-167444600 Weak transcription Right Atrium heart
5 chr5:167441800-167446400 Strong transcription Foreskin Keratinocyte Primary Cells skin02 Skin
6 chr5:167442600-167444600 Strong transcription NHEK skin
7 chr5:167442600-167446000 Weak transcription Fetal Brain Male brain
8 chr5:167443000-167444200 Strong transcription Foreskin Keratinocyte Primary Cells skin03 Skin
9 chr5:167443000-167444600 Weak transcription Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells embryonic stem cell
10 chr5:167443000-167449200 Weak transcription Breast variant Human Mammary Epithelial Cells (vHMEC) Breast
11 chr5:167443200-167447400 Weak transcription Bone Marrow Derived Cultured Mesenchymal Stem Cells Bone marrow
12 chr5:167443200-167452000 Weak transcription HSMM muscle
13 chr5:167443600-167444800 Enhancers Right Ventricle heart
14 chr5:167443800-167466000 Weak transcription H9 Derived Neuron Cultured Cells ES cell derived
15 chr5:167444000-167444800 Enhancers Left Ventricle heart
16 chr5:167444000-167449600 Weak transcription Breast Myoepithelial Primary Cells Breast

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