Variant report

Variant	rs2167042
Chromosome Location	chr3:34586158-34586159
allele	C/T
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]
rs11129598	0.93[AMR][1000 genomes];0.89[EUR][1000 genomes]
rs13074645	0.81[AMR][1000 genomes]
rs1520641	0.90[AFR][1000 genomes];0.93[AMR][1000 genomes]
rs1520644	0.93[AMR][1000 genomes]
rs1851057	0.86[AMR][1000 genomes]
rs2167041	0.84[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs2336653	0.93[AMR][1000 genomes];0.86[EUR][1000 genomes]
rs4678695	0.93[AMR][1000 genomes];0.81[EUR][1000 genomes]
rs6798617	0.81[AMR][1000 genomes];0.89[EUR][1000 genomes]
rs7614078	0.93[AMR][1000 genomes];0.89[EUR][1000 genomes]
rs7629903	0.81[AMR][1000 genomes];0.81[EUR][1000 genomes]
rs918085	0.87[AMR][1000 genomes]
rs9860621	0.83[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	nsv1007906	chr3:34466966-34607465	ZNF genes & repeats Active TSS Enhancers Weak transcription Flanking Active TSS Strong transcription	TF binding region 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	chr3:34585200-34586400	Enhancers	Primary monocytes fromperipheralblood	blood

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

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