Variant report

Variant	rs415536
Chromosome Location	chr1:45591389-45591390
allele	C/T
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 93 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:88)

rs_ID	r²[population]
rs10789454	0.90[EUR][1000 genomes]
rs11211074	0.88[AMR][1000 genomes];0.96[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs1144868	1.00[AFR][1000 genomes];0.97[AMR][1000 genomes];0.99[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs11806438	1.00[ASN][1000 genomes]
rs11810239	0.98[ASN][1000 genomes]
rs1226670	1.00[ASN][1000 genomes]
rs1226733	0.98[ASN][1000 genomes]
rs1226734	0.98[ASN][1000 genomes]
rs1226735	0.83[ASN][1000 genomes]
rs1226746	1.00[ASN][1000 genomes]
rs1226747	1.00[ASN][1000 genomes]
rs1226748	1.00[ASN][1000 genomes]
rs1226836	0.85[AMR][1000 genomes];0.87[EUR][1000 genomes];0.86[ASN][1000 genomes]
rs1226914	0.98[AFR][1000 genomes];0.91[AMR][1000 genomes];0.94[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs1782459	0.97[ASN][1000 genomes]
rs1938300	0.98[AFR][1000 genomes];0.88[AMR][1000 genomes];0.95[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs1938301	0.98[AFR][1000 genomes];0.88[AMR][1000 genomes];0.95[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs1938303	1.00[ASN][1000 genomes]
rs1938304	0.98[AFR][1000 genomes];0.88[AMR][1000 genomes];0.93[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs1938407	0.87[AFR][1000 genomes];0.85[EUR][1000 genomes]
rs2088956	0.98[ASN][1000 genomes]
rs2105458	0.99[AFR][1000 genomes];0.88[AMR][1000 genomes];0.95[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs2186219	0.89[AFR][1000 genomes];0.85[EUR][1000 genomes]
rs2356302	0.98[AFR][1000 genomes];0.88[AMR][1000 genomes];0.95[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs238249	0.94[AFR][1000 genomes];1.00[AMR][1000 genomes];0.99[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs2997458	0.82[AFR][1000 genomes];0.84[EUR][1000 genomes]
rs2997461	0.92[AFR][1000 genomes];0.81[AMR][1000 genomes];0.87[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs2997465	0.99[AFR][1000 genomes];0.94[AMR][1000 genomes];0.95[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs3009968	0.94[AFR][1000 genomes];0.94[AMR][1000 genomes];0.95[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs3009969	0.99[AFR][1000 genomes];0.94[AMR][1000 genomes];0.95[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs3009974	0.98[AFR][1000 genomes];0.88[AMR][1000 genomes];0.95[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs3009979	0.92[AFR][1000 genomes];0.87[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs3121732	0.89[AFR][1000 genomes];0.85[EUR][1000 genomes]
rs3121769	0.87[AFR][1000 genomes];0.85[EUR][1000 genomes]
rs34134455	1.00[ASN][1000 genomes]
rs346684	1.00[ASN][1000 genomes]
rs346687	0.99[AFR][1000 genomes];0.97[AMR][1000 genomes];1.00[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs346693	1.00[ASN][1000 genomes]
rs346695	1.00[ASN][1000 genomes]
rs346696	1.00[AFR][1000 genomes];0.94[AMR][1000 genomes];0.99[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs346697	1.00[ASN][1000 genomes]
rs346698	1.00[ASN][1000 genomes]
rs346700	1.00[ASN][1000 genomes]
rs346701	0.84[AFR][1000 genomes];0.92[AMR][1000 genomes];0.95[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs346702	1.00[ASN][1000 genomes]
rs346705	1.00[ASN][1000 genomes]
rs346706	1.00[ASN][1000 genomes]
rs346707	1.00[ASN][1000 genomes]
rs346708	0.92[ASN][1000 genomes]
rs346712	1.00[ASN][1000 genomes]
rs346716	1.00[ASN][1000 genomes]
rs346717	1.00[ASN][1000 genomes]
rs346719	1.00[ASN][1000 genomes]
rs346721	1.00[ASN][1000 genomes]
rs346723	0.98[AFR][1000 genomes];0.94[AMR][1000 genomes];0.99[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs346724	1.00[ASN][1000 genomes]
rs346729	1.00[ASN][1000 genomes]
rs346731	0.94[AFR][1000 genomes];0.98[AMR][1000 genomes];0.93[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs346732	1.00[ASN][1000 genomes]
rs346733	0.98[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs346734	1.00[ASN][1000 genomes]
rs346735	1.00[ASN][1000 genomes]
rs346736	0.98[AFR][1000 genomes];1.00[AMR][1000 genomes];0.99[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs346737	0.98[AFR][1000 genomes];1.00[AMR][1000 genomes];0.99[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs3738246	0.98[ASN][1000 genomes]
rs3850855	0.82[AMR][1000 genomes];0.97[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs3850856	1.00[ASN][1000 genomes]
rs4454584	0.97[AFR][1000 genomes];0.89[AMR][1000 genomes];0.93[EUR][1000 genomes];0.82[ASN][1000 genomes]
rs454624	1.00[ASN][1000 genomes]
rs4660295	1.00[ASN][1000 genomes]
rs4660834	0.98[ASN][1000 genomes]
rs4660839	1.00[ASN][1000 genomes]
rs4660841	1.00[ASN][1000 genomes]
rs55932948	0.80[ASN][1000 genomes]
rs56086213	0.80[ASN][1000 genomes]
rs56363452	1.00[ASN][1000 genomes]
rs56791336	1.00[ASN][1000 genomes]
rs57754814	0.80[ASN][1000 genomes]
rs58374842	1.00[ASN][1000 genomes]
rs58934647	1.00[ASN][1000 genomes]
rs59220391	0.90[ASN][1000 genomes]
rs61789780	1.00[ASN][1000 genomes]
rs61789781	1.00[ASN][1000 genomes]
rs6429557	0.88[AMR][1000 genomes];0.98[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs6688318	0.98[ASN][1000 genomes]
rs6702327	0.98[ASN][1000 genomes]
rs72684493	1.00[ASN][1000 genomes]
rs974143	1.00[ASN][1000 genomes]

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	nsv529677	chr1:45179509-45748571	Weak transcription Enhancers ZNF genes & repeats Strong transcription Flanking Active TSS Active TSS Genic enhancers Bivalent/Poised TSS Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	424 gene(s)	inside rSNPs	diseases
2	nsv1002026	chr1:45187594-45758048	Flanking Active TSS Enhancers Genic enhancers Strong transcription Weak transcription Bivalent/Poised TSS Transcr. at gene 5' and 3' ZNF genes & repeats Flanking Bivalent TSS/Enh Active TSS Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	386 gene(s)	inside rSNPs	diseases
3	nsv915644	chr1:45282802-45696079	Enhancers Genic enhancers Strong transcription Flanking Active TSS Weak transcription Flanking Bivalent TSS/Enh Active TSS Bivalent Enhancer Transcr. at gene 5' and 3' Bivalent/Poised TSS ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	98 gene(s)	inside rSNPs	diseases
4	nsv498036	chr1:45428030-46050934	Active TSS Enhancers Flanking Active TSS Genic enhancers Weak transcription Strong transcription Bivalent/Poised TSS Transcr. at gene 5' and 3' ZNF genes & repeats Flanking Bivalent TSS/Enh Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	191 gene(s)	inside rSNPs	diseases
5	nsv546148	chr1:45500294-45627663	Weak transcription Enhancers Strong transcription ZNF genes & repeats Flanking Active TSS Genic enhancers Active TSS Bivalent Enhancer Flanking Bivalent TSS/Enh Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA	10 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	chr1:45568200-45594600	Weak transcription	Right Atrium	heart
2	chr1:45590000-45627000	Weak transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
3	chr1:45591200-45591600	Weak transcription	HepG2	liver

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