Variant report

Variant	rs10139105
Chromosome Location	chr14:63311194-63311195
allele	C/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 78 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:77)

rs_ID	r²[population]
rs10047851	1.00[CEU][hapmap];1.00[CHB][hapmap];0.90[JPT][hapmap]
rs10047852	1.00[CEU][hapmap];1.00[CHB][hapmap];0.90[JPT][hapmap]
rs10047856	1.00[CEU][hapmap];1.00[CHB][hapmap];0.90[JPT][hapmap]
rs10047884	1.00[CEU][hapmap];1.00[CHB][hapmap];0.90[JPT][hapmap]
rs10047938	1.00[CEU][hapmap];1.00[CHB][hapmap];0.90[JPT][hapmap]
rs10130817	1.00[CEU][hapmap];1.00[CHB][hapmap];0.90[JPT][hapmap]
rs10134277	0.88[EUR][1000 genomes]
rs10134985	0.90[CHB][hapmap]
rs10135128	1.00[CEU][hapmap];0.85[CHB][hapmap]
rs10135421	0.81[CEU][hapmap];0.90[CHB][hapmap]
rs10135862	0.90[CEU][hapmap];0.94[CHB][hapmap]
rs10136167	1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];1.00[YRI][hapmap]
rs10138498	1.00[CEU][hapmap];1.00[CHB][hapmap];0.86[JPT][hapmap]
rs10139268	1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];1.00[YRI][hapmap]
rs10139468	1.00[CEU][hapmap];1.00[CHB][hapmap];0.90[JPT][hapmap]
rs10140008	1.00[CEU][hapmap];1.00[CHB][hapmap];0.90[JPT][hapmap]
rs10143260	0.91[EUR][1000 genomes];0.81[ASN][1000 genomes]
rs10143966	0.88[EUR][1000 genomes]
rs10146526	1.00[CEU][hapmap];1.00[CHB][hapmap];0.90[JPT][hapmap]
rs10146673	1.00[CEU][hapmap]
rs10146879	0.90[CEU][hapmap];0.90[CHB][hapmap]
rs10147931	1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];1.00[YRI][hapmap]
rs10148076	1.00[CEU][hapmap];1.00[CHB][hapmap];0.90[JPT][hapmap]
rs10483757	1.00[CEU][hapmap];1.00[CHB][hapmap];0.90[JPT][hapmap]
rs10483758	0.81[CEU][hapmap];1.00[CHB][hapmap];0.90[JPT][hapmap];1.00[YRI][hapmap]
rs10483759	0.90[CEU][hapmap];0.89[CHB][hapmap]
rs10483760	0.90[CEU][hapmap]
rs10483762	0.89[CHB][hapmap]
rs10873163	1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];1.00[YRI][hapmap]
rs10873164	0.90[CHB][hapmap]
rs10873165	0.90[CEU][hapmap];0.90[CHB][hapmap]
rs12100661	1.00[CEU][hapmap];0.95[CHB][hapmap];0.86[JPT][hapmap]
rs12147279	0.94[CHB][hapmap]
rs12586807	0.90[CEU][hapmap];0.89[CHB][hapmap]
rs12587225	0.90[CEU][hapmap];0.84[CHB][hapmap]
rs12587258	0.90[CEU][hapmap];0.84[CHB][hapmap]
rs12588293	0.90[CHB][hapmap]
rs12588552	0.89[CHB][hapmap]
rs12588586	0.90[CHB][hapmap]
rs12589408	0.90[CEU][hapmap]
rs12881527	0.89[CHB][hapmap]
rs1543437	0.90[CEU][hapmap];0.89[CHB][hapmap]
rs17100446	1.00[CEU][hapmap];1.00[CHB][hapmap];0.90[JPT][hapmap]
rs17100497	0.90[CHB][hapmap]
rs17223580	1.00[CEU][hapmap];0.89[CHB][hapmap];0.93[EUR][1000 genomes];0.81[ASN][1000 genomes]
rs17223818	0.90[CEU][hapmap]
rs17223839	0.90[CEU][hapmap]
rs17223846	0.90[CEU][hapmap];0.90[CHB][hapmap]
rs17823609	1.00[CEU][hapmap];0.89[CHB][hapmap];0.91[EUR][1000 genomes];0.81[ASN][1000 genomes]
rs17823627	0.81[CEU][hapmap];0.90[CHB][hapmap]
rs17823807	0.90[CEU][hapmap];0.90[CHB][hapmap]
rs1950568	1.00[CEU][hapmap];1.00[CHB][hapmap];0.90[JPT][hapmap]
rs1956018	1.00[CEU][hapmap];1.00[CHB][hapmap];0.90[JPT][hapmap]
rs1956026	0.90[CEU][hapmap]
rs2355741	0.81[CEU][hapmap];1.00[CHB][hapmap];0.90[JPT][hapmap]
rs243163	0.81[CEU][hapmap]
rs2860089	1.00[CEU][hapmap];1.00[CHB][hapmap];0.85[JPT][hapmap]
rs41419249	1.00[CEU][hapmap];1.00[CHB][hapmap];0.90[JPT][hapmap];1.00[YRI][hapmap]
rs4146434	0.90[CEU][hapmap]
rs4146435	0.90[CEU][hapmap]
rs4270090	0.90[CEU][hapmap];0.89[CHB][hapmap]
rs4899096	1.00[CEU][hapmap];1.00[CHB][hapmap];0.90[JPT][hapmap]
rs4899100	0.81[CEU][hapmap];0.89[CHB][hapmap]
rs4902191	1.00[CEU][hapmap];0.90[CHB][hapmap]
rs4902192	0.90[CEU][hapmap];0.94[CHB][hapmap];1.00[YRI][hapmap]
rs4902193	0.90[CEU][hapmap];0.89[CHB][hapmap]
rs6573462	0.90[CHB][hapmap]
rs7146868	0.89[CHB][hapmap]
rs8004918	0.88[CEU][hapmap];0.89[CHB][hapmap]
rs8005915	0.81[CEU][hapmap];0.89[CHB][hapmap]
rs8007782	0.90[CEU][hapmap]
rs8013931	0.90[CHB][hapmap]
rs8015097	0.90[CHB][hapmap]
rs9323421	1.00[CEU][hapmap];1.00[CHB][hapmap];0.90[JPT][hapmap]
rs9323422	1.00[CEU][hapmap];1.00[CHB][hapmap];0.90[JPT][hapmap]
rs9888566	1.00[CEU][hapmap];0.89[CHB][hapmap]
rs9888605	1.00[CEU][hapmap];0.90[CHB][hapmap]

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	nsv902015	chr14:63261862-63356253	Enhancers Weak transcription ZNF genes & repeats Strong 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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