Variant report

Variant	rs73650726
Chromosome Location	chr9:85152666-85152667
allele	A/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 13 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:12)

rs_ID	r²[population]
rs60422971	0.82[AFR][1000 genomes];1.00[EUR][1000 genomes]
rs6559669	0.85[AFR][1000 genomes];1.00[EUR][1000 genomes]
rs7027542	1.00[EUR][1000 genomes]
rs7045382	0.82[AFR][1000 genomes];1.00[EUR][1000 genomes]
rs73648484	1.00[EUR][1000 genomes]
rs73648486	1.00[EUR][1000 genomes]
rs73650724	0.85[AFR][1000 genomes];1.00[EUR][1000 genomes]
rs73650725	0.87[AFR][1000 genomes];1.00[EUR][1000 genomes]
rs73650727	0.87[AFR][1000 genomes];1.00[EUR][1000 genomes]
rs73650728	0.82[AFR][1000 genomes];1.00[EUR][1000 genomes]
rs73650729	1.00[EUR][1000 genomes]
rs7857253	1.00[EUR][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:1 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv831641	chr9:85145561-85309589	Enhancers ZNF genes & repeats Weak transcription Bivalent Enhancer Flanking Active TSS Active TSS Bivalent/Poised TSS	Chromatin interactive region lncRNA	3 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:2 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr9:85150600-85161000	Weak transcription	Fetal Lung	lung
2	chr9:85150800-85155200	Weak transcription	Primary hematopoietic stem cells short term culture	blood

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dbSNP/dbVar ID: rs12345 /nsv7879
a single nucleotide as 0-based coordinates: chr1:12345
chromosomal regions: chr1:12345-34567

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