Variant report

Variant	rs73650735
Chromosome Location	chr9:85188721-85188722
allele	A/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 15 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:14)

rs_ID	r²[population]
rs59370555	1.00[EUR][1000 genomes]
rs60180321	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs60533521	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs7021753	1.00[EUR][1000 genomes]
rs7035647	1.00[EUR][1000 genomes]
rs7035686	1.00[EUR][1000 genomes]
rs73648457	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs73648459	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs73648461	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs73648488	1.00[EUR][1000 genomes]
rs73650743	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs7846939	1.00[EUR][1000 genomes]
rs7854783	1.00[EUR][1000 genomes]
rs7868675	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:1 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr9:85188400-85189000	Enhancers	HepG2	liver

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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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