Variant report

Variant rs59662117
Chromosome Location chr5:167468627-167468628
allele C/T
Outlinks Ensembl   UCSC
Chromatin state (count:14 , 50 per page) page: 1
No. Chromosome Location Chromatin state Cell line Tissue
1 chr5:167447600-167483000 Weak transcription Right Atrium heart
2 chr5:167450800-167474000 Weak transcription Left Ventricle heart
3 chr5:167455200-167474600 Weak transcription NHEK skin
4 chr5:167457400-167469000 Weak transcription Breast Myoepithelial Primary Cells Breast
5 chr5:167458200-167474200 Weak transcription Bone Marrow Derived Cultured Mesenchymal Stem Cells Bone marrow
6 chr5:167463800-167470800 Strong transcription Foreskin Keratinocyte Primary Cells skin02 Skin
7 chr5:167465400-167469000 Weak transcription Right Ventricle heart
8 chr5:167465400-167473000 Weak transcription Foreskin Keratinocyte Primary Cells skin03 Skin
9 chr5:167465800-167470200 Enhancers hESC Derived CD56+ Ectoderm Cultured Cells ES cell derived
10 chr5:167466800-167470000 Enhancers hESC Derived CD184+ Endoderm Cultured Cells ES cell derived
11 chr5:167467000-167473200 Weak transcription H1 Derived Mesenchymal Stem Cells ES cell derived
12 chr5:167467200-167474000 Weak transcription H1 Derived Neuronal Progenitor Cultured Cells ES cell derived
13 chr5:167468000-167500800 Weak transcription Breast variant Human Mammary Epithelial Cells (vHMEC) Breast
14 chr5:167468400-167469000 Bivalent Enhancer Fetal Brain Male brain

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