Variant report

Variant	rs58302722
Chromosome Location	chr4:127415516-127415517
allele	A/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 14 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:13)

rs_ID	r²[population]
rs10857114	0.90[AMR][1000 genomes];0.84[EUR][1000 genomes]
rs11098875	0.90[AMR][1000 genomes];0.81[EUR][1000 genomes]
rs11098877	0.90[AMR][1000 genomes];0.87[EUR][1000 genomes]
rs11098878	0.99[ASN][1000 genomes]
rs12498989	0.90[AMR][1000 genomes];0.84[EUR][1000 genomes]
rs12501073	0.90[AMR][1000 genomes];0.87[EUR][1000 genomes]
rs12641163	0.90[AMR][1000 genomes];0.87[EUR][1000 genomes]
rs12643879	0.90[AMR][1000 genomes];0.84[EUR][1000 genomes]
rs12650259	0.87[EUR][1000 genomes]
rs57902647	0.88[ASN][1000 genomes]
rs61193656	0.90[AMR][1000 genomes];0.87[EUR][1000 genomes]
rs6820218	0.87[EUR][1000 genomes]
rs6840101	0.87[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	nsv595385	chr4:127383473-127451806	Weak transcription Enhancers ZNF genes & repeats Strong transcription Flanking Active TSS Genic enhancers Active TSS	Chromatin interactive region	n/a	inside rSNPs	n/a

No data

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

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr4:127414200-127415800	Weak transcription	K562	blood

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dbSNP/dbVar ID: rs12345 /nsv7879
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chromosomal regions: chr1:12345-34567

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