Variant report

Variant	rs8013931
Chromosome Location	chr14:63338563-63338564
allele	A/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 82 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:80)

rs_ID	r²[population]
rs10047851	0.90[CHB][hapmap];0.81[JPT][hapmap]
rs10047852	0.90[CHB][hapmap];0.81[JPT][hapmap]
rs10047856	0.90[CHB][hapmap];0.81[JPT][hapmap]
rs10047884	0.90[CHB][hapmap];0.81[JPT][hapmap]
rs10047938	0.90[CHB][hapmap];0.81[JPT][hapmap]
rs10130817	0.90[CHB][hapmap];0.81[JPT][hapmap]
rs10134277	0.95[ASN][1000 genomes]
rs10134985	1.00[CHB][hapmap];1.00[JPT][hapmap]
rs10135128	0.95[CHB][hapmap];0.87[JPT][hapmap]
rs10135421	0.93[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap]
rs10135862	0.86[CEU][hapmap];1.00[CHB][hapmap];0.82[JPT][hapmap]
rs10136167	0.90[CHB][hapmap]
rs10138498	0.90[CHB][hapmap]
rs10139105	0.90[CHB][hapmap]
rs10139268	0.90[CHB][hapmap];0.80[JPT][hapmap]
rs10139468	0.90[CHB][hapmap];0.81[JPT][hapmap]
rs10140008	0.90[CHB][hapmap];0.81[JPT][hapmap]
rs10143260	0.95[ASN][1000 genomes]
rs10143966	0.95[ASN][1000 genomes]
rs10146526	0.90[CHB][hapmap];0.82[JPT][hapmap]
rs10146879	0.86[CEU][hapmap];1.00[CHB][hapmap];0.87[JPT][hapmap]
rs10147931	0.90[CHB][hapmap]
rs10148076	0.90[CHB][hapmap];0.82[JPT][hapmap]
rs10151264	0.83[AMR][1000 genomes];0.91[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs10483757	0.90[CHB][hapmap];0.82[JPT][hapmap]
rs10483758	0.90[CHB][hapmap];0.81[JPT][hapmap]
rs10483759	0.85[CEU][hapmap];1.00[CHB][hapmap];0.90[ASN][1000 genomes]
rs10483760	0.85[CEU][hapmap]
rs10483762	1.00[CHB][hapmap];0.87[JPT][hapmap];0.82[ASN][1000 genomes]
rs10873163	0.90[CHB][hapmap]
rs10873164	1.00[CHB][hapmap];0.87[JPT][hapmap]
rs10873165	0.86[CEU][hapmap];1.00[CHB][hapmap];0.87[JPT][hapmap]
rs12100661	0.85[CHB][hapmap]
rs12147279	1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap]
rs12586807	0.85[CEU][hapmap];1.00[CHB][hapmap];0.86[JPT][hapmap]
rs12587225	0.85[CEU][hapmap];0.95[CHB][hapmap];0.81[ASN][1000 genomes]
rs12587258	0.86[CEU][hapmap];0.95[CHB][hapmap];0.81[ASN][1000 genomes]
rs12588293	1.00[CHB][hapmap];0.87[JPT][hapmap]
rs12588552	0.87[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap]
rs12588586	1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap]
rs12589408	0.85[CEU][hapmap]
rs12881527	1.00[CHB][hapmap];0.87[JPT][hapmap];0.88[ASN][1000 genomes]
rs1543437	0.85[CEU][hapmap];1.00[CHB][hapmap];0.86[JPT][hapmap]
rs17100446	0.90[CHB][hapmap];0.81[JPT][hapmap]
rs17100497	1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap]
rs17223580	1.00[CHB][hapmap];0.91[JPT][hapmap];0.95[ASN][1000 genomes]
rs17223818	0.86[CEU][hapmap]
rs17223839	0.85[CEU][hapmap]
rs17223846	0.85[CEU][hapmap];1.00[CHB][hapmap]
rs17823609	0.85[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];0.95[ASN][1000 genomes]
rs17823627	0.93[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap]
rs17823807	0.86[CEU][hapmap];1.00[CHB][hapmap]
rs1950568	0.90[CHB][hapmap];0.82[JPT][hapmap]
rs1956018	0.90[CHB][hapmap];0.81[JPT][hapmap]
rs1956026	0.86[CEU][hapmap]
rs2144775	0.94[ASN][1000 genomes]
rs2355741	0.90[CHB][hapmap];0.81[JPT][hapmap]
rs2860089	0.90[CHB][hapmap]
rs41419249	0.90[CHB][hapmap];0.81[JPT][hapmap]
rs4146434	0.85[CEU][hapmap]
rs4146435	0.85[CEU][hapmap]
rs4270090	0.85[CEU][hapmap];1.00[CHB][hapmap];0.86[JPT][hapmap]
rs4899096	0.90[CHB][hapmap];0.81[JPT][hapmap]
rs4899100	0.93[CEU][hapmap];1.00[CHB][hapmap];0.95[JPT][hapmap];0.83[AMR][1000 genomes];0.91[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs4902191	1.00[CHB][hapmap];0.87[JPT][hapmap]
rs4902192	0.85[CEU][hapmap];0.90[CHB][hapmap]
rs4902193	0.85[CEU][hapmap];1.00[CHB][hapmap];0.86[JPT][hapmap]
rs57087381	0.90[ASN][1000 genomes]
rs59454582	0.89[ASN][1000 genomes]
rs6573462	1.00[CHB][hapmap];1.00[JPT][hapmap]
rs7146868	1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];0.96[YRI][hapmap]
rs8004918	0.84[CEU][hapmap];1.00[CHB][hapmap]
rs8005915	0.93[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];1.00[YRI][hapmap]
rs8007782	0.86[CEU][hapmap]
rs8015097	1.00[CHB][hapmap];1.00[JPT][hapmap];0.97[ASN][1000 genomes]
rs8019236	0.90[CHB][hapmap]
rs9323421	0.89[CHB][hapmap];0.81[JPT][hapmap]
rs9323422	0.90[CHB][hapmap];0.82[JPT][hapmap]
rs9888566	1.00[CHB][hapmap];0.86[JPT][hapmap]
rs9888605	1.00[CHB][hapmap];0.87[JPT][hapmap]

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	nsv902015	chr14:63261862-63356253	Enhancers Weak transcription ZNF genes & repeats Strong transcription	Chromatin interactive region	n/a	inside rSNPs	diseases
2	nsv1042953	chr14:63314591-63384260	Enhancers Weak transcription	Chromatin interactive region	n/a	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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