Variant report

Variant	rs1418845
Chromosome Location	chr1:158479691-158479692
allele	A/C
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 141 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:139)

rs_ID	r²[population]
rs1032352	0.99[ASN][1000 genomes]
rs10489834	1.00[CEU][hapmap]
rs10489835	1.00[CEU][hapmap]
rs10797010	0.96[ASN][1000 genomes]
rs10797011	0.99[ASN][1000 genomes]
rs10797012	0.99[ASN][1000 genomes]
rs10797013	0.99[ASN][1000 genomes]
rs10797017	1.00[CEU][hapmap]
rs10797022	0.99[ASN][1000 genomes]
rs10797023	0.99[ASN][1000 genomes]
rs10797024	0.99[ASN][1000 genomes]
rs10908651	0.96[ASN][1000 genomes]
rs10908652	0.89[AMR][1000 genomes];0.90[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs10908653	0.96[ASN][1000 genomes]
rs10908654	0.95[ASN][1000 genomes]
rs10908655	0.98[ASN][1000 genomes]
rs10908656	0.98[ASN][1000 genomes]
rs10908657	0.99[ASN][1000 genomes]
rs10908658	0.99[ASN][1000 genomes]
rs10908659	0.89[AMR][1000 genomes];0.93[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs10908660	0.99[ASN][1000 genomes]
rs10908661	0.99[ASN][1000 genomes]
rs10908663	0.99[ASN][1000 genomes]
rs10908664	0.94[AMR][1000 genomes];0.95[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs10908680	1.00[CEU][hapmap]
rs1112915	0.96[ASN][1000 genomes]
rs11264976	0.94[ASN][1000 genomes]
rs11264977	0.96[ASN][1000 genomes]
rs11264978	0.96[ASN][1000 genomes]
rs11264981	0.96[ASN][1000 genomes]
rs11264983	0.98[ASN][1000 genomes]
rs11264984	0.99[ASN][1000 genomes]
rs11264985	0.99[ASN][1000 genomes]
rs11264987	0.99[ASN][1000 genomes]
rs11264988	0.99[ASN][1000 genomes]
rs11264989	0.95[CEU][hapmap]
rs11264994	0.90[AMR][1000 genomes];0.90[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs11264997	1.00[ASN][1000 genomes]
rs11264998	1.00[CEU][hapmap]
rs11265002	1.00[CEU][hapmap]
rs1157523	0.89[AMR][1000 genomes];0.91[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs1157525	0.96[ASN][1000 genomes]
rs12034004	0.99[ASN][1000 genomes]
rs12041218	1.00[CEU][hapmap]
rs12044283	0.99[ASN][1000 genomes]
rs12044288	0.99[ASN][1000 genomes]
rs12075903	0.98[ASN][1000 genomes]
rs12078065	0.99[ASN][1000 genomes]
rs12080815	1.00[CEU][hapmap];0.92[EUR][1000 genomes];0.86[ASN][1000 genomes]
rs12081915	1.00[CEU][hapmap];0.92[EUR][1000 genomes];0.86[ASN][1000 genomes]
rs12118446	0.99[ASN][1000 genomes]
rs12122663	0.97[ASN][1000 genomes]
rs12133791	0.97[ASN][1000 genomes]
rs12133794	0.97[ASN][1000 genomes]
rs12145401	0.99[ASN][1000 genomes]
rs12403685	0.96[ASN][1000 genomes]
rs1342946	0.96[ASN][1000 genomes]
rs1342947	0.99[ASN][1000 genomes]
rs1342949	0.89[ASN][1000 genomes]
rs1342950	0.99[ASN][1000 genomes]
rs1342952	0.99[ASN][1000 genomes]
rs1342953	0.99[ASN][1000 genomes]
rs1342954	0.99[ASN][1000 genomes]
rs1342958	1.00[CEU][hapmap]
rs1418843	0.89[AMR][1000 genomes];0.90[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs1418844	0.95[ASN][1000 genomes]
rs1418846	1.00[CEU][hapmap];0.99[AMR][1000 genomes];0.99[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs1418847	1.00[CEU][hapmap];0.97[AMR][1000 genomes];0.99[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs1491196	0.89[AMR][1000 genomes];0.94[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs1578761	0.99[ASN][1000 genomes]
rs1578762	0.99[ASN][1000 genomes]
rs1578763	0.99[ASN][1000 genomes]
rs17630699	0.89[AMR][1000 genomes];0.94[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs1873509	0.98[ASN][1000 genomes]
rs1873510	0.98[ASN][1000 genomes]
rs1873511	0.98[ASN][1000 genomes]
rs1894038	0.96[ASN][1000 genomes]
rs1894040	0.96[ASN][1000 genomes]
rs2023632	0.98[ASN][1000 genomes]
rs2051450	0.97[ASN][1000 genomes]
rs2051451	0.99[ASN][1000 genomes]
rs2157687	0.99[ASN][1000 genomes]
rs2157689	0.89[AMR][1000 genomes];0.94[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs2213947	0.88[AMR][1000 genomes];0.90[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs2220633	0.96[ASN][1000 genomes]
rs2317969	0.99[ASN][1000 genomes]
rs2317970	0.97[ASN][1000 genomes]
rs2873593	0.97[ASN][1000 genomes]
rs2873594	0.97[ASN][1000 genomes]
rs2873595	0.97[ASN][1000 genomes]
rs4276920	0.97[ASN][1000 genomes]
rs4373761	0.99[ASN][1000 genomes]
rs4575081	0.97[ASN][1000 genomes]
rs4609418	0.99[ASN][1000 genomes]
rs4614256	0.99[ASN][1000 genomes]
rs57366633	0.96[ASN][1000 genomes]
rs6427438	0.96[ASN][1000 genomes]
rs6427439	0.98[ASN][1000 genomes]
rs6657638	0.99[ASN][1000 genomes]
rs6663277	0.99[ASN][1000 genomes]
rs6664542	0.98[ASN][1000 genomes]
rs6666609	0.99[ASN][1000 genomes]
rs6670343	0.99[ASN][1000 genomes]
rs6672789	0.99[ASN][1000 genomes]
rs6674656	0.99[ASN][1000 genomes]
rs6679056	0.96[ASN][1000 genomes]
rs6689657	0.98[ASN][1000 genomes]
rs6697656	0.89[ASN][1000 genomes]
rs6699473	0.99[ASN][1000 genomes]
rs7514555	0.96[ASN][1000 genomes]
rs7514968	0.99[ASN][1000 genomes]
rs7515245	0.99[ASN][1000 genomes]
rs7518708	0.97[ASN][1000 genomes]
rs7518808	0.99[ASN][1000 genomes]
rs7525362	0.99[ASN][1000 genomes]
rs7526514	0.92[EUR][1000 genomes];0.86[ASN][1000 genomes]
rs7533071	0.97[ASN][1000 genomes]
rs7540999	0.97[ASN][1000 genomes]
rs7548349	0.99[ASN][1000 genomes]
rs7549123	0.96[ASN][1000 genomes]
rs7551497	0.96[ASN][1000 genomes]
rs7555174	1.00[ASN][1000 genomes]
rs863345	1.00[CEU][hapmap];0.92[EUR][1000 genomes];0.85[ASN][1000 genomes]
rs863346	0.92[EUR][1000 genomes];0.85[ASN][1000 genomes]
rs863347	0.96[CEU][hapmap];0.92[EUR][1000 genomes];0.85[ASN][1000 genomes]
rs863351	1.00[CEU][hapmap];0.92[EUR][1000 genomes];0.85[ASN][1000 genomes]
rs863352	1.00[CEU][hapmap];0.92[EUR][1000 genomes];0.85[ASN][1000 genomes]
rs863353	0.92[EUR][1000 genomes];0.85[ASN][1000 genomes]
rs863356	0.92[EUR][1000 genomes];0.85[ASN][1000 genomes]
rs863365	0.93[CEU][hapmap]
rs879635	0.98[ASN][1000 genomes]
rs879637	0.98[ASN][1000 genomes]
rs923663	0.97[ASN][1000 genomes]
rs923664	0.97[ASN][1000 genomes]
rs949397	0.98[ASN][1000 genomes]
rs949398	0.98[ASN][1000 genomes]
rs950260	0.99[ASN][1000 genomes]
rs950487	0.98[ASN][1000 genomes]
rs9804005	0.82[AMR][1000 genomes];0.92[EUR][1000 genomes];0.89[ASN][1000 genomes]

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	nsv872479	chr1:158118787-158484285	Active TSS Enhancers Bivalent Enhancer Flanking Active TSS Weak transcription Transcr. at gene 5' and 3' Bivalent/Poised TSS ZNF genes & repeats Flanking Bivalent TSS/Enh Strong transcription Genic enhancers	TF binding region CpG island Chromatin interactive region lncRNA	18 gene(s)	inside rSNPs	diseases
2	nsv1001046	chr1:158461563-158503338	Bivalent Enhancer Enhancers Transcr. at gene 5' and 3' Weak transcription Flanking Active TSS Active TSS	TF binding region CpG island Chromatin interactive region lncRNA	4 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:3 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr1:158479600-158480000	Enhancers	Fetal Adrenal Gland	Adrenal Gland
2	chr1:158479600-158480200	Enhancers	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
3	chr1:158479600-158480200	Enhancers	Fetal Stomach	stomach

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