Variant report

Variant	rs1520449
Chromosome Location	chr2:50606741-50606742
allele	C/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 63 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:58)

rs_ID	r²[population]
rs10181522	0.95[CEU][hapmap];1.00[CHB][hapmap];0.95[JPT][hapmap];0.85[AMR][1000 genomes];0.93[EUR][1000 genomes];0.92[ASN][1000 genomes]
rs10182951	0.80[EUR][1000 genomes]
rs10184843	0.90[CEU][hapmap];0.87[CHB][hapmap];0.95[JPT][hapmap];1.00[YRI][hapmap]
rs10188271	0.95[CEU][hapmap];1.00[CHB][hapmap];0.95[JPT][hapmap]
rs10191261	0.95[CEU][hapmap];0.91[CHB][hapmap];0.86[JPT][hapmap]
rs10201390	0.91[CEU][hapmap];0.87[CHB][hapmap];0.86[JPT][hapmap];0.91[YRI][hapmap]
rs10203960	0.91[CEU][hapmap];0.87[CHB][hapmap];0.86[JPT][hapmap]
rs10205311	0.95[CEU][hapmap];1.00[CHB][hapmap];0.86[JPT][hapmap];0.83[AMR][1000 genomes];0.92[EUR][1000 genomes];0.88[ASN][1000 genomes]
rs10209627	0.88[AMR][1000 genomes];0.93[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs10210660	0.95[CEU][hapmap];0.86[JPT][hapmap]
rs10490228	0.91[CHB][hapmap];0.86[JPT][hapmap];0.91[YRI][hapmap];0.85[AMR][1000 genomes];0.95[ASN][1000 genomes]
rs12465784	0.90[AMR][1000 genomes];0.93[EUR][1000 genomes];0.92[ASN][1000 genomes]
rs12467043	0.91[CEU][hapmap];0.83[CHB][hapmap];0.95[JPT][hapmap]
rs12475464	0.95[CEU][hapmap]
rs12475979	0.95[CEU][hapmap];0.91[CHB][hapmap];0.90[JPT][hapmap];0.85[AMR][1000 genomes];0.90[EUR][1000 genomes];0.86[ASN][1000 genomes]
rs12476139	0.81[AMR][1000 genomes];0.87[EUR][1000 genomes]
rs12619946	0.80[EUR][1000 genomes]
rs12620045	0.80[EUR][1000 genomes]
rs12713097	1.00[CEU][hapmap];0.91[CHB][hapmap];0.95[JPT][hapmap];0.84[AFR][1000 genomes];0.91[AMR][1000 genomes];0.95[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs12713098	0.91[CHB][hapmap];0.95[JPT][hapmap];0.86[AMR][1000 genomes];0.96[ASN][1000 genomes]
rs12713100	0.80[AMR][1000 genomes]
rs12994492	0.91[CHB][hapmap];0.81[JPT][hapmap];0.91[YRI][hapmap];0.92[ASN][1000 genomes]
rs13005521	0.95[CEU][hapmap]
rs13014058	0.95[CEU][hapmap];0.91[CHB][hapmap];0.86[JPT][hapmap]
rs13014624	0.96[CHB][hapmap];0.95[JPT][hapmap]
rs13032292	0.84[AMR][1000 genomes];0.94[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs13032775	1.00[CEU][hapmap];0.91[CHB][hapmap];0.95[JPT][hapmap];0.88[AMR][1000 genomes];0.93[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs13382506	1.00[CEU][hapmap];0.91[CHB][hapmap];0.95[JPT][hapmap]
rs13392422	0.95[CEU][hapmap];0.91[CHB][hapmap];0.95[JPT][hapmap]
rs13421278	0.95[CEU][hapmap];0.91[CHB][hapmap];0.86[JPT][hapmap]
rs13430295	0.95[CEU][hapmap];0.87[CHB][hapmap];0.95[JPT][hapmap];0.91[YRI][hapmap]
rs13430435	0.95[CEU][hapmap];0.91[CHB][hapmap];0.95[JPT][hapmap]
rs1402124	1.00[CEU][hapmap];1.00[CHB][hapmap];0.95[JPT][hapmap]
rs1402128	0.85[JPT][hapmap]
rs1520443	0.95[CEU][hapmap];0.91[CHB][hapmap];0.95[JPT][hapmap]
rs1520446	1.00[CEU][hapmap];0.96[CHB][hapmap];0.95[JPT][hapmap]
rs1533692	0.83[AMR][1000 genomes];0.87[EUR][1000 genomes];0.87[ASN][1000 genomes]
rs17040569	0.87[CHB][hapmap];0.95[JPT][hapmap];0.84[AMR][1000 genomes];0.97[ASN][1000 genomes]
rs17040577	0.91[CHB][hapmap];0.81[JPT][hapmap];0.83[YRI][hapmap];0.84[AMR][1000 genomes];0.93[ASN][1000 genomes]
rs17040600	0.95[CEU][hapmap];0.91[CHB][hapmap];0.95[JPT][hapmap]
rs17040640	0.80[EUR][1000 genomes]
rs1818714	1.00[CEU][hapmap];1.00[CHB][hapmap];0.95[JPT][hapmap]
rs1818715	0.95[CEU][hapmap];1.00[CHB][hapmap];0.95[JPT][hapmap]
rs1818716	0.95[CEU][hapmap];1.00[CHB][hapmap];0.95[JPT][hapmap]
rs1851015	1.00[CEU][hapmap];0.95[CHB][hapmap];0.86[JPT][hapmap]
rs2160443	0.80[EUR][1000 genomes]
rs2351517	0.91[CEU][hapmap];0.87[CHB][hapmap];0.86[JPT][hapmap]
rs34846571	0.80[EUR][1000 genomes]
rs4638832	0.84[AMR][1000 genomes];0.83[EUR][1000 genomes];0.82[ASN][1000 genomes]
rs57564327	0.81[AMR][1000 genomes];0.91[EUR][1000 genomes];0.85[ASN][1000 genomes]
rs6709416	0.91[CEU][hapmap];0.87[CHB][hapmap];0.95[JPT][hapmap]
rs6711307	0.80[EUR][1000 genomes]
rs6743117	0.80[EUR][1000 genomes]
rs6743584	0.80[EUR][1000 genomes]
rs7567375	0.90[CEU][hapmap];0.95[JPT][hapmap]
rs7581097	0.91[CEU][hapmap]
rs7585229	0.80[EUR][1000 genomes]
rs939402	0.95[CEU][hapmap];1.00[CHB][hapmap];0.95[JPT][hapmap]

Variant overlapped rSNPs/rCNVs (count:5 , 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

No data

Chromatin state (count:1 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr2:50606200-50606800	Enhancers	H9 Derived Neuron Cultured Cells	ES cell derived

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