Variant report

Variant	rs1520446
Chromosome Location	chr2:50604829-50604830
allele	G/T
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 58 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:52)

rs_ID	r²[population]
rs10181522	0.95[CEU][hapmap];0.95[CHB][hapmap];1.00[JPT][hapmap];0.93[EUR][1000 genomes];0.91[ASN][1000 genomes]
rs10184843	0.90[CEU][hapmap];0.83[CHB][hapmap];1.00[JPT][hapmap]
rs10188271	0.95[CEU][hapmap];0.95[CHB][hapmap];1.00[JPT][hapmap]
rs10191195	0.80[CHB][hapmap]
rs10191261	0.95[CEU][hapmap];0.95[CHB][hapmap];0.90[JPT][hapmap]
rs10201390	0.91[CEU][hapmap];0.83[CHB][hapmap];0.90[JPT][hapmap]
rs10203960	0.91[CEU][hapmap];0.83[CHB][hapmap];0.90[JPT][hapmap]
rs10205311	0.95[CEU][hapmap];0.95[CHB][hapmap];0.90[JPT][hapmap];0.80[AMR][1000 genomes];0.93[EUR][1000 genomes];0.86[ASN][1000 genomes]
rs10209627	0.80[AMR][1000 genomes];0.94[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs10210660	0.95[CEU][hapmap];0.83[CHB][hapmap];0.90[JPT][hapmap]
rs10490228	0.95[CHB][hapmap];0.90[JPT][hapmap];0.80[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs12465784	0.86[AMR][1000 genomes];0.94[EUR][1000 genomes];0.92[ASN][1000 genomes]
rs12467043	0.91[CEU][hapmap];0.87[CHB][hapmap];1.00[JPT][hapmap]
rs12475464	0.95[CEU][hapmap]
rs12475979	0.95[CEU][hapmap];0.86[CHB][hapmap];0.95[JPT][hapmap];0.81[AMR][1000 genomes];0.91[EUR][1000 genomes];0.86[ASN][1000 genomes]
rs12476139	0.87[EUR][1000 genomes]
rs12613343	0.80[EUR][1000 genomes]
rs12713097	1.00[CEU][hapmap];0.95[CHB][hapmap];1.00[JPT][hapmap];0.83[AMR][1000 genomes];0.96[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs12713098	0.95[CHB][hapmap];1.00[JPT][hapmap];0.80[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs12994492	0.95[CHB][hapmap];0.85[JPT][hapmap];0.93[ASN][1000 genomes]
rs13005521	0.95[CEU][hapmap];0.81[YRI][hapmap]
rs13014058	0.95[CEU][hapmap];0.95[CHB][hapmap];0.90[JPT][hapmap]
rs13014624	0.91[CHB][hapmap];1.00[JPT][hapmap]
rs13032292	0.95[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs13032775	1.00[CEU][hapmap];0.95[CHB][hapmap];1.00[JPT][hapmap];0.80[AMR][1000 genomes];0.94[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs13382506	1.00[CEU][hapmap];0.95[CHB][hapmap];1.00[JPT][hapmap]
rs13392422	0.95[CEU][hapmap];0.95[CHB][hapmap];1.00[JPT][hapmap]
rs13421278	0.95[CEU][hapmap];0.95[CHB][hapmap];0.90[JPT][hapmap]
rs13430295	0.95[CEU][hapmap];0.83[CHB][hapmap];1.00[JPT][hapmap]
rs13430435	0.95[CEU][hapmap];0.95[CHB][hapmap];1.00[JPT][hapmap]
rs1402124	1.00[CEU][hapmap];0.95[CHB][hapmap];1.00[JPT][hapmap]
rs1402128	0.82[CHB][hapmap];0.90[JPT][hapmap];1.00[YRI][hapmap]
rs1520438	0.80[EUR][1000 genomes]
rs1520443	0.95[CEU][hapmap];0.95[CHB][hapmap];1.00[JPT][hapmap]
rs1520449	1.00[CEU][hapmap];0.96[CHB][hapmap];0.95[JPT][hapmap];0.91[AMR][1000 genomes];0.99[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs1533692	0.87[EUR][1000 genomes];0.86[ASN][1000 genomes]
rs17040569	0.91[CHB][hapmap];1.00[JPT][hapmap];0.80[AMR][1000 genomes];0.99[ASN][1000 genomes]
rs17040577	0.95[CHB][hapmap];0.86[JPT][hapmap];0.81[EUR][1000 genomes];0.94[ASN][1000 genomes]
rs17040600	0.95[CEU][hapmap];0.95[CHB][hapmap];1.00[JPT][hapmap]
rs1818714	1.00[CEU][hapmap];0.95[CHB][hapmap];1.00[JPT][hapmap]
rs1818715	0.95[CEU][hapmap];0.95[CHB][hapmap];1.00[JPT][hapmap]
rs1818716	0.95[CEU][hapmap];0.95[CHB][hapmap];1.00[JPT][hapmap]
rs1851015	1.00[CEU][hapmap];1.00[CHB][hapmap];0.90[JPT][hapmap]
rs2351517	0.91[CEU][hapmap];0.83[CHB][hapmap];0.90[JPT][hapmap];0.96[YRI][hapmap]
rs4638832	0.80[AMR][1000 genomes];0.84[EUR][1000 genomes];0.82[ASN][1000 genomes]
rs57564327	0.92[EUR][1000 genomes];0.84[ASN][1000 genomes]
rs6709416	0.91[CEU][hapmap];0.83[CHB][hapmap];1.00[JPT][hapmap]
rs6709865	0.80[EUR][1000 genomes]
rs6738086	0.80[EUR][1000 genomes]
rs7567375	0.90[CEU][hapmap];0.82[CHB][hapmap];1.00[JPT][hapmap]
rs7581097	0.91[CEU][hapmap];0.84[YRI][hapmap]
rs939402	0.95[CEU][hapmap];0.96[CHB][hapmap];1.00[JPT][hapmap]

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	nsv932915	chr2:50306630-50628415	Flanking Active TSS Active TSS Flanking Bivalent TSS/Enh Enhancers Bivalent/Poised TSS Weak transcription Bivalent Enhancer ZNF genes & repeats Strong transcription	TF binding region CpG island Chromatin interactive region	2 gene(s)	inside rSNPs	diseases
2	nsv492164	chr2:50399251-51029090	Enhancers Flanking Active TSS Weak transcription Flanking Bivalent TSS/Enh Active TSS Bivalent/Poised TSS Bivalent Enhancer ZNF genes & repeats Strong transcription Genic enhancers	TF binding region CpG island Chromatin interactive region lncRNA	4 gene(s)	inside rSNPs	diseases
3	nsv1000653	chr2:50417660-51083470	Enhancers Flanking Active TSS Active TSS Weak transcription ZNF genes & repeats Bivalent Enhancer Flanking Bivalent TSS/Enh Bivalent/Poised TSS Strong transcription Genic enhancers	TF binding region CpG island Chromatin interactive region lncRNA	5 gene(s)	inside rSNPs	diseases
4	nsv535693	chr2:50417660-51083470	Enhancers Weak transcription Bivalent Enhancer ZNF genes & repeats Strong transcription Flanking Active TSS Active TSS Bivalent/Poised TSS Flanking Bivalent TSS/Enh Genic enhancers	TF binding region CpG island Chromatin interactive region lncRNA	5 gene(s)	inside rSNPs	diseases
5	nsv948548	chr2:50569117-50695100	Flanking Bivalent TSS/Enh Bivalent Enhancer Weak transcription Flanking Active TSS Enhancers Active TSS Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region	1 gene(s)	inside rSNPs	diseases
6	esv2762560	chr2:50597915-50605863	Enhancers	n/a	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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