Variant report

Variant	rs17547284
Chromosome Location	chr11:56310356-56310357
allele	A/T
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 89 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:83)

rs_ID	r²[population]
rs10501355	0.94[AMR][1000 genomes];0.85[EUR][1000 genomes]
rs11228735	1.00[JPT][hapmap]
rs12270384	1.00[YRI][hapmap]
rs17150695	1.00[JPT][hapmap]
rs17542961	1.00[CEU][hapmap]
rs17546536	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs17547207	1.00[CEU][hapmap];1.00[YRI][hapmap]
rs17547542	1.00[CEU][hapmap]
rs17547806	1.00[CEU][hapmap]
rs17548679	0.94[AMR][1000 genomes];0.94[EUR][1000 genomes]
rs17548700	1.00[AMR][1000 genomes];0.88[EUR][1000 genomes]
rs17548819	1.00[CEU][hapmap]
rs17549606	0.91[CEU][hapmap];0.94[AMR][1000 genomes];0.82[EUR][1000 genomes]
rs17614327	1.00[CEU][hapmap]
rs17627302	1.00[CEU][hapmap];0.97[EUR][1000 genomes]
rs17628586	1.00[CEU][hapmap];0.98[EUR][1000 genomes]
rs17628691	0.81[AMR][1000 genomes];0.98[EUR][1000 genomes]
rs17629033	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs17629218	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs17629804	1.00[CEU][hapmap];1.00[YRI][hapmap]
rs17629861	1.00[CEU][hapmap]
rs17630028	1.00[CEU][hapmap]
rs17630040	0.91[CEU][hapmap]
rs1807254	0.81[AMR][1000 genomes];0.98[EUR][1000 genomes]
rs1876924	1.00[CEU][hapmap]
rs1945237	1.00[CEU][hapmap]
rs1945262	1.00[CEU][hapmap]
rs55771448	0.81[AMR][1000 genomes];0.98[EUR][1000 genomes]
rs55874240	1.00[AMR][1000 genomes];0.85[EUR][1000 genomes]
rs56078926	1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs56163075	0.81[AMR][1000 genomes];0.97[EUR][1000 genomes]
rs56394926	0.81[AMR][1000 genomes];0.92[EUR][1000 genomes]
rs61901983	0.97[EUR][1000 genomes]
rs61902021	0.98[EUR][1000 genomes]
rs61902022	0.98[EUR][1000 genomes]
rs61902171	1.00[AMR][1000 genomes];0.97[EUR][1000 genomes]
rs61902203	1.00[AMR][1000 genomes];0.97[EUR][1000 genomes]
rs61902209	1.00[AMR][1000 genomes];0.97[EUR][1000 genomes]
rs61902863	0.98[EUR][1000 genomes]
rs61902883	0.81[AMR][1000 genomes];0.98[EUR][1000 genomes]
rs61902885	0.81[AMR][1000 genomes];0.98[EUR][1000 genomes]
rs61902915	0.81[AMR][1000 genomes];0.98[EUR][1000 genomes]
rs61902916	0.81[AMR][1000 genomes];0.98[EUR][1000 genomes]
rs61902921	0.81[AMR][1000 genomes];0.98[EUR][1000 genomes]
rs61903268	1.00[AMR][1000 genomes];0.94[EUR][1000 genomes]
rs61903273	1.00[AMR][1000 genomes];0.94[EUR][1000 genomes]
rs61903306	1.00[AMR][1000 genomes];0.94[EUR][1000 genomes]
rs61903313	1.00[AMR][1000 genomes];0.85[EUR][1000 genomes]
rs61903315	0.94[AMR][1000 genomes];0.85[EUR][1000 genomes]
rs61903316	0.88[AMR][1000 genomes];0.84[EUR][1000 genomes]
rs61903320	0.94[AMR][1000 genomes];0.85[EUR][1000 genomes]
rs61903321	0.94[AMR][1000 genomes];0.85[EUR][1000 genomes]
rs61903347	1.00[AMR][1000 genomes];0.85[EUR][1000 genomes]
rs61903530	0.86[EUR][1000 genomes]
rs61903531	0.86[EUR][1000 genomes]
rs61903536	0.86[EUR][1000 genomes]
rs61903537	0.86[EUR][1000 genomes]
rs61903541	0.86[EUR][1000 genomes]
rs61904062	1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs61904063	1.00[AMR][1000 genomes];0.97[EUR][1000 genomes]
rs61904064	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs61904562	0.94[AMR][1000 genomes];0.82[EUR][1000 genomes]
rs61904563	0.94[AMR][1000 genomes];0.82[EUR][1000 genomes]
rs61904564	0.87[AMR][1000 genomes]
rs61904565	0.81[AMR][1000 genomes]
rs61904579	0.88[AMR][1000 genomes]
rs61904584	0.88[AMR][1000 genomes]
rs61904586	0.88[AMR][1000 genomes]
rs61904587	0.83[AMR][1000 genomes]
rs6591380	1.00[CEU][hapmap];1.00[AMR][1000 genomes];0.94[EUR][1000 genomes]
rs7103598	0.97[EUR][1000 genomes]
rs7111634	1.00[CEU][hapmap]
rs7114870	1.00[CEU][hapmap];0.94[EUR][1000 genomes]
rs7121991	1.00[CEU][hapmap];0.81[AMR][1000 genomes];0.98[EUR][1000 genomes]
rs7123108	1.00[CEU][hapmap]
rs7126549	0.98[EUR][1000 genomes]
rs7130906	0.87[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs7925450	1.00[CEU][hapmap]
rs7927015	0.91[CEU][hapmap]
rs7935533	1.00[CEU][hapmap]
rs7939771	0.94[AMR][1000 genomes];0.85[EUR][1000 genomes]
rs7942730	1.00[CEU][hapmap]
rs7951506	0.98[EUR][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:6 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv1050024	chr11:55900482-56518943	Enhancers Weak transcription ZNF genes & repeats Flanking Active TSS Active TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA	52 gene(s)	inside rSNPs	diseases
2	nsv497854	chr11:55917298-56537994	Enhancers ZNF genes & repeats Active TSS Weak transcription Flanking Active TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA	50 gene(s)	inside rSNPs	diseases
3	nsv971949	chr11:56126625-56344170	Enhancers Weak transcription ZNF genes & repeats Active TSS	TF binding region CpG island Chromatin interactive region	18 gene(s)	inside rSNPs	diseases
4	nsv1046487	chr11:56228761-56310644	Enhancers Weak transcription	TF binding region CpG island Chromatin interactive region	9 gene(s)	inside rSNPs	diseases
5	nsv468576	chr11:56299930-56420029	Weak transcription Flanking Active TSS Enhancers Active TSS	TF binding region CpG island Chromatin interactive region lncRNA	10 gene(s)	inside rSNPs	diseases
6	nsv555099	chr11:56299930-56420029	Enhancers Active TSS Weak transcription Flanking Active TSS	TF binding region CpG island Chromatin interactive region lncRNA	10 gene(s)	inside rSNPs	diseases

No data

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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