Variant report

Variant rs12347783
Chromosome Location chr9:108533137-108533138
allele A/T
Outlinks Ensembl   UCSC
Chromatin state (count:13 , 50 per page) page: 1
No. Chromosome Location Chromatin state Cell line Tissue
1 chr9:108514000-108540000 Weak transcription HSMMtube muscle
2 chr9:108515200-108545000 Weak transcription K562 blood
3 chr9:108515200-108560600 Weak transcription Ovary ovary
4 chr9:108515400-108536800 Weak transcription H1 Derived Neuronal Progenitor Cultured Cells ES cell derived
5 chr9:108515600-108538600 Weak transcription H9 Derived Neuron Cultured Cells ES cell derived
6 chr9:108517800-108538400 Weak transcription H9 Derived Neuronal Progenitor Cultured Cells ES cell derived
7 chr9:108520600-108535200 Weak transcription Primary hematopoietic stem cells blood
8 chr9:108520600-108546400 Weak transcription Fetal Intestine Small intestine
9 chr9:108521000-108534200 Weak transcription Primary hematopoietic stem cells short term culture blood
10 chr9:108521000-108538400 Weak transcription Primary B cells from cord blood blood
11 chr9:108529000-108534400 Weak transcription Primary hematopoietic stem cells G-CSF-mobilized Male --
12 chr9:108530400-108552600 Weak transcription Pancreas Pancrea
13 chr9:108533000-108537000 Weak transcription Breast variant Human Mammary Epithelial Cells (vHMEC) Breast

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