Variant report

Variant rs34118922
Chromosome Location chr5:167493124-167493125
allele A/G
Outlinks Ensembl   UCSC
Chromatin state (count:13 , 50 per page) page: 1
No. Chromosome Location Chromatin state Cell line Tissue
1 chr5:167468000-167500800 Weak transcription Breast variant Human Mammary Epithelial Cells (vHMEC) Breast
2 chr5:167483200-167502400 Weak transcription Fetal Heart heart
3 chr5:167488400-167496800 Strong transcription Foreskin Keratinocyte Primary Cells skin03 Skin
4 chr5:167489200-167494000 Strong transcription NHEK skin
5 chr5:167491600-167494800 Weak transcription Right Ventricle heart
6 chr5:167491800-167494000 Weak transcription Breast Myoepithelial Primary Cells Breast
7 chr5:167491800-167494600 Weak transcription Left Ventricle heart
8 chr5:167491800-167500600 Weak transcription HSMM muscle
9 chr5:167491800-167509200 Weak transcription H9 Derived Neuron Cultured Cells ES cell derived
10 chr5:167492000-167494600 Weak transcription H1 Derived Mesenchymal Stem Cells ES cell derived
11 chr5:167492000-167500600 Weak transcription NH-A brain
12 chr5:167492200-167493200 Weak transcription Bone Marrow Derived Cultured Mesenchymal Stem Cells Bone marrow
13 chr5:167492800-167497400 Strong transcription Foreskin Keratinocyte Primary Cells skin02 Skin

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