Variant report

Variant rs17069767
Chromosome Location chr5:167490933-167490934
allele A/G
Outlinks Ensembl   UCSC
Chromatin state (count:17 , 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 chr5:167474600-167491400 Weak transcription H1 Derived Mesenchymal Stem Cells ES cell derived
3 chr5:167475000-167491800 Weak transcription NH-A brain
4 chr5:167483200-167502400 Weak transcription Fetal Heart heart
5 chr5:167488400-167496800 Strong transcription Foreskin Keratinocyte Primary Cells skin03 Skin
6 chr5:167488600-167491400 Weak transcription Primary hematopoietic stem cells G-CSF-mobilized Female --
7 chr5:167488600-167491400 Weak transcription Primary hematopoietic stem cells G-CSF-mobilized Male --
8 chr5:167488600-167491400 Weak transcription Liver Liver
9 chr5:167488800-167491200 Strong transcription H9 Derived Neuron Cultured Cells ES cell derived
10 chr5:167489000-167492200 Strong transcription Bone Marrow Derived Cultured Mesenchymal Stem Cells Bone marrow
11 chr5:167489200-167491800 Strong transcription Breast Myoepithelial Primary Cells Breast
12 chr5:167489200-167491800 Strong transcription HSMM muscle
13 chr5:167489200-167492200 Strong transcription Foreskin Keratinocyte Primary Cells skin02 Skin
14 chr5:167489200-167494000 Strong transcription NHEK skin
15 chr5:167489400-167491800 Weak transcription H9 Derived Neuronal Progenitor Cultured Cells ES cell derived
16 chr5:167490000-167491200 Weak transcription Left Ventricle heart
17 chr5:167490600-167492000 Enhancers Fetal Lung lung

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