Variant report

Variant rs17497547
Chromosome Location chr22:22890792-22890793
allele C/T
Outlinks Ensembl   UCSC
Chromatin state (count:12 , 50 per page) page: 1
No. Chromosome Location Chromatin state Cell line Tissue
1 chr22:22887400-22897000 Weak transcription Primary T helper memory cells from peripheral blood 2 blood
2 chr22:22887800-22890800 Enhancers Primary monocytes fromperipheralblood blood
3 chr22:22887800-22890800 Enhancers Monocytes-CD14+_RO01746 blood
4 chr22:22888000-22890800 Enhancers Primary hematopoietic stem cells short term culture blood
5 chr22:22888400-22891000 Enhancers Primary hematopoietic stem cells blood
6 chr22:22888400-22891000 Enhancers Primary hematopoietic stem cells G-CSF-mobilized Female --
7 chr22:22888400-22891000 Enhancers Primary hematopoietic stem cells G-CSF-mobilized Male --
8 chr22:22889000-22891000 Strong transcription Right Atrium heart
9 chr22:22889000-22894000 Genic enhancers K562 blood
10 chr22:22889000-22896600 Strong transcription A549 lung
11 chr22:22890600-22890800 Bivalent Enhancer Adipose Nuclei Adipose
12 chr22:22890600-22891000 Active TSS Brain Substantia Nigra brain

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