Variant report

Variant	rs11123027
Chromosome Location	chr2:124957592-124957593
allele	A/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 53 )
Associated
traits (count: 2 )

rSNPs within LD-proxies of this variant (count:51)

rs_ID	r²[population]
rs10496634	0.94[CEU][hapmap];0.91[EUR][1000 genomes]
rs11679836	0.91[EUR][1000 genomes]
rs11682281	0.94[CEU][hapmap];0.91[EUR][1000 genomes]
rs11682449	0.84[AMR][1000 genomes];0.92[EUR][1000 genomes]
rs11695218	0.86[AMR][1000 genomes];0.92[EUR][1000 genomes]
rs1170602	1.00[CEU][hapmap]
rs1170607	0.85[ASW][hapmap];1.00[CEU][hapmap];1.00[GIH][hapmap];0.91[MEX][hapmap];0.95[MKK][hapmap];1.00[TSI][hapmap];0.86[YRI][hapmap]
rs1170611	1.00[ASW][hapmap];1.00[CEU][hapmap];1.00[GIH][hapmap];0.94[LWK][hapmap];1.00[MEX][hapmap];0.98[MKK][hapmap];1.00[TSI][hapmap];1.00[YRI][hapmap]
rs1170612	1.00[CEU][hapmap]
rs1170619	1.00[CEU][hapmap];0.85[YRI][hapmap];0.91[AMR][1000 genomes];0.96[EUR][1000 genomes]
rs1170621	1.00[CEU][hapmap];0.85[YRI][hapmap];0.89[AMR][1000 genomes];0.96[EUR][1000 genomes]
rs1170626	0.85[ASW][hapmap];1.00[CEU][hapmap];1.00[GIH][hapmap];0.91[MEX][hapmap];0.95[MKK][hapmap];1.00[TSI][hapmap];0.86[YRI][hapmap]
rs1170630	1.00[CEU][hapmap]
rs1170634	1.00[CEU][hapmap];1.00[YRI][hapmap]
rs1170636	0.80[EUR][1000 genomes]
rs1184930	0.93[CEU][hapmap];0.93[AMR][1000 genomes];0.95[EUR][1000 genomes]
rs11891838	0.84[AMR][1000 genomes];0.92[EUR][1000 genomes]
rs11899935	0.94[CEU][hapmap];1.00[GIH][hapmap];0.93[TSI][hapmap];0.89[EUR][1000 genomes]
rs11902121	0.94[CEU][hapmap];1.00[GIH][hapmap];0.91[MEX][hapmap];0.93[TSI][hapmap];0.84[AMR][1000 genomes];0.92[EUR][1000 genomes]
rs11902656	0.94[CEU][hapmap]
rs12473278	0.91[AMR][1000 genomes];0.99[EUR][1000 genomes]
rs12473309	1.00[AFR][1000 genomes];0.98[AMR][1000 genomes];0.99[EUR][1000 genomes]
rs12986451	0.85[EUR][1000 genomes]
rs12987836	0.84[AMR][1000 genomes];0.92[EUR][1000 genomes]
rs13033123	0.94[CEU][hapmap]
rs13033298	0.92[CEU][hapmap]
rs13033474	0.94[CEU][hapmap];1.00[GIH][hapmap];0.90[TSI][hapmap]
rs1529298	0.94[CEU][hapmap];0.86[AMR][1000 genomes];0.92[EUR][1000 genomes]
rs1529299	0.94[CEU][hapmap];1.00[GIH][hapmap];0.91[MEX][hapmap];0.93[TSI][hapmap];0.86[AMR][1000 genomes];0.93[EUR][1000 genomes]
rs17011004	0.94[CEU][hapmap];0.90[EUR][1000 genomes]
rs17011031	0.94[CEU][hapmap];0.91[EUR][1000 genomes]
rs17011040	0.94[CEU][hapmap];1.00[GIH][hapmap];0.91[MEX][hapmap];0.93[TSI][hapmap];0.84[AMR][1000 genomes];0.91[EUR][1000 genomes]
rs17011058	0.94[CEU][hapmap];0.82[AMR][1000 genomes];0.92[EUR][1000 genomes]
rs2699359	1.00[CEU][hapmap]
rs2699360	1.00[CEU][hapmap]
rs35122611	0.86[AMR][1000 genomes];0.93[EUR][1000 genomes]
rs4848919	1.00[CEU][hapmap];1.00[GIH][hapmap];0.91[MEX][hapmap];1.00[TSI][hapmap];0.91[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs4848920	1.00[ASW][hapmap];1.00[CEU][hapmap];1.00[GIH][hapmap];0.94[LWK][hapmap];1.00[MEX][hapmap];1.00[MKK][hapmap];1.00[TSI][hapmap];1.00[YRI][hapmap]
rs56321724	0.91[EUR][1000 genomes]
rs56369586	0.91[EUR][1000 genomes]
rs57578864	0.86[AMR][1000 genomes];0.92[EUR][1000 genomes]
rs62163932	0.91[EUR][1000 genomes]
rs62163933	0.84[AMR][1000 genomes];0.92[EUR][1000 genomes]
rs62163934	0.84[AMR][1000 genomes];0.92[EUR][1000 genomes]
rs749196	1.00[CEU][hapmap];0.91[AMR][1000 genomes];0.95[EUR][1000 genomes]
rs7561523	0.94[CEU][hapmap];1.00[GIH][hapmap];0.93[TSI][hapmap];0.84[AMR][1000 genomes];0.92[EUR][1000 genomes]
rs7561939	0.88[CEU][hapmap];1.00[GIH][hapmap];0.91[MEX][hapmap];0.93[TSI][hapmap];0.86[AMR][1000 genomes];0.85[EUR][1000 genomes]
rs7571024	1.00[CEU][hapmap];1.00[YRI][hapmap]
rs7584334	0.84[AMR][1000 genomes];0.92[EUR][1000 genomes]
rs7594531	1.00[CEU][hapmap];1.00[YRI][hapmap]
rs7598484	0.84[AMR][1000 genomes];0.92[EUR][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:2 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv531408	chr2:124727329-125011247	Bivalent Enhancer Enhancers Bivalent/Poised TSS Flanking Active TSS Flanking Bivalent TSS/Enh Weak transcription Active TSS ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA	2 gene(s)	inside rSNPs	diseases
2	nsv874989	chr2:124892592-125176030	Enhancers ZNF genes & repeats Weak transcription Active TSS Flanking Active TSS Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA	1 gene(s)	inside rSNPs	diseases

mRNA abundance (count:2)

SNP	Gene	Cis/trans	Tissue	Source
rs11123027	APOBEC2	trans	parietal	SCAN
rs11123027	CYP27C1	cis	cerebellum	SCAN

Chromatin state (count:0 , 50 per page) page:

No data

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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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