Variant report

Variant	rs1483353
Chromosome Location	chr8:85489629-85489630
allele	C/T
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 109 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:107)

rs_ID	r²[population]
rs10089129	0.82[CEU][hapmap]
rs10093758	0.85[EUR][1000 genomes]
rs10094897	1.00[JPT][hapmap]
rs10096903	0.81[CEU][hapmap]
rs10104232	1.00[JPT][hapmap]
rs10105150	0.82[CEU][hapmap]
rs10109730	1.00[JPT][hapmap]
rs10112163	0.85[CEU][hapmap]
rs10504807	0.95[CEU][hapmap];1.00[JPT][hapmap]
rs10504808	1.00[CEU][hapmap];1.00[JPT][hapmap]
rs10958225	1.00[CEU][hapmap];1.00[JPT][hapmap]
rs11985369	0.91[CEU][hapmap]
rs11989750	0.85[CEU][hapmap]
rs1252199	0.95[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];0.96[YRI][hapmap]
rs1252200	1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];0.86[YRI][hapmap];0.93[AMR][1000 genomes];0.97[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs1252202	0.90[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];0.85[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs1252204	1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];0.90[YRI][hapmap];0.97[AMR][1000 genomes];0.99[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs1252205	0.95[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];0.93[YRI][hapmap];0.86[AFR][1000 genomes];0.99[AMR][1000 genomes];0.99[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs1252208	1.00[CHB][hapmap];1.00[JPT][hapmap];0.96[YRI][hapmap];0.96[AFR][1000 genomes];0.97[AMR][1000 genomes];0.97[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs1252209	1.00[CHB][hapmap];1.00[JPT][hapmap];0.86[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs1252210	0.95[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];0.88[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs1252211	0.94[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];0.93[YRI][hapmap];0.93[AFR][1000 genomes];0.99[AMR][1000 genomes];1.00[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs1252212	1.00[CHB][hapmap];1.00[JPT][hapmap];0.96[YRI][hapmap];0.94[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs1252213	0.99[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs1252215	1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap]
rs1252216	1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];0.86[YRI][hapmap]
rs1252217	0.91[CEU][hapmap];1.00[CHB][hapmap];0.91[JPT][hapmap]
rs1252219	0.93[CHB][hapmap];1.00[JPT][hapmap];0.96[YRI][hapmap]
rs1252220	0.86[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs1252221	1.00[CEU][hapmap];0.92[CHB][hapmap];1.00[JPT][hapmap];0.85[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs1252222	0.86[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs1252223	1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];0.97[YRI][hapmap]
rs1252224	0.95[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap]
rs1252225	0.95[CEU][hapmap];1.00[JPT][hapmap];0.91[AMR][1000 genomes];0.99[EUR][1000 genomes];0.94[ASN][1000 genomes]
rs1268561	0.86[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs1268562	0.95[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];0.88[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs1351724	0.95[CEU][hapmap];1.00[JPT][hapmap];0.86[EUR][1000 genomes];0.92[ASN][1000 genomes]
rs1466522	0.95[CEU][hapmap];1.00[JPT][hapmap];0.84[AMR][1000 genomes];0.96[EUR][1000 genomes];0.95[ASN][1000 genomes]
rs1483354	1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];0.88[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs1488706	0.91[CEU][hapmap]
rs1488709	1.00[JPT][hapmap]
rs1565225	0.82[CEU][hapmap]
rs1626630	0.99[AFR][1000 genomes];0.99[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs1681355	1.00[CEU][hapmap];0.84[CHB][hapmap];1.00[JPT][hapmap];0.86[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs16912908	0.81[JPT][hapmap]
rs16913056	1.00[CEU][hapmap];1.00[JPT][hapmap];0.84[AMR][1000 genomes];0.97[EUR][1000 genomes];0.91[ASN][1000 genomes]
rs16913090	1.00[CEU][hapmap];1.00[JPT][hapmap];0.84[AMR][1000 genomes];0.92[EUR][1000 genomes];0.91[ASN][1000 genomes]
rs1730816	1.00[CHB][hapmap];1.00[JPT][hapmap];0.97[YRI][hapmap];0.94[AFR][1000 genomes];0.97[AMR][1000 genomes];0.99[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs1730824	0.98[AFR][1000 genomes];0.99[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs1730826	0.88[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs1730827	1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];0.97[YRI][hapmap];0.97[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs17726976	0.81[CEU][hapmap]
rs17794266	1.00[CEU][hapmap];0.82[CHB][hapmap];1.00[JPT][hapmap]
rs17794302	1.00[JPT][hapmap];0.83[EUR][1000 genomes];0.91[ASN][1000 genomes]
rs17794614	1.00[CEU][hapmap];1.00[JPT][hapmap]
rs1842962	0.95[CEU][hapmap];1.00[JPT][hapmap];0.91[AMR][1000 genomes];0.97[EUR][1000 genomes];0.94[ASN][1000 genomes]
rs2220426	0.95[CEU][hapmap];0.91[JPT][hapmap];0.80[YRI][hapmap]
rs2467210	0.82[CEU][hapmap]
rs2634055	0.82[CEU][hapmap]
rs2634056	0.82[CEU][hapmap]
rs2634057	0.82[CEU][hapmap]
rs2634059	0.82[CEU][hapmap]
rs2634061	0.82[CEU][hapmap]
rs2634066	0.82[CEU][hapmap]
rs2634067	0.84[CEU][hapmap]
rs2718968	0.84[CEU][hapmap]
rs2718970	0.82[CEU][hapmap]
rs2718971	0.82[CEU][hapmap]
rs2718972	0.82[CEU][hapmap]
rs2718984	0.82[CEU][hapmap]
rs2718986	0.82[CEU][hapmap]
rs2718987	0.82[CEU][hapmap]
rs28405987	0.86[EUR][1000 genomes];0.80[ASN][1000 genomes]
rs28446816	0.87[AMR][1000 genomes];0.96[EUR][1000 genomes];0.95[ASN][1000 genomes]
rs28676726	0.81[EUR][1000 genomes];0.86[ASN][1000 genomes]
rs28695582	0.86[AMR][1000 genomes];0.91[EUR][1000 genomes];0.95[ASN][1000 genomes]
rs28760488	0.84[EUR][1000 genomes];0.91[ASN][1000 genomes]
rs2930064	0.86[EUR][1000 genomes];0.95[ASN][1000 genomes]
rs2930065	0.95[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];0.96[YRI][hapmap]
rs2957790	1.00[CHB][hapmap];1.00[JPT][hapmap];0.82[AFR][1000 genomes];0.97[AMR][1000 genomes];0.99[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs2970009	1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap]
rs3101802	0.81[JPT][hapmap]
rs3109781	1.00[ASN][1000 genomes]
rs4302839	1.00[CEU][hapmap];1.00[JPT][hapmap];0.80[AMR][1000 genomes];0.87[EUR][1000 genomes];0.87[ASN][1000 genomes]
rs4416819	1.00[JPT][hapmap]
rs56165928	0.81[EUR][1000 genomes];0.89[ASN][1000 genomes]
rs56335539	0.83[EUR][1000 genomes];0.91[ASN][1000 genomes]
rs66683633	0.91[ASN][1000 genomes]
rs6986632	0.91[CEU][hapmap]
rs6988126	0.86[CEU][hapmap]
rs6997041	1.00[CEU][hapmap];1.00[JPT][hapmap];0.84[AMR][1000 genomes];0.93[EUR][1000 genomes];0.89[ASN][1000 genomes]
rs7010348	1.00[CEU][hapmap];1.00[JPT][hapmap]
rs7014897	1.00[CEU][hapmap];1.00[JPT][hapmap];0.81[EUR][1000 genomes];0.89[ASN][1000 genomes]
rs72681013	0.86[ASN][1000 genomes]
rs729076	0.95[CEU][hapmap];1.00[JPT][hapmap]
rs7815917	0.91[CEU][hapmap]
rs7819269	1.00[CEU][hapmap];1.00[JPT][hapmap];0.84[EUR][1000 genomes];0.91[ASN][1000 genomes]
rs7820496	0.80[EUR][1000 genomes]
rs7828076	0.95[CEU][hapmap];1.00[JPT][hapmap]
rs7831433	0.91[CEU][hapmap]
rs7840920	0.95[CEU][hapmap];1.00[JPT][hapmap]
rs7840925	1.00[JPT][hapmap]
rs7841984	0.95[CEU][hapmap];1.00[JPT][hapmap]
rs7842614	1.00[CEU][hapmap];1.00[JPT][hapmap]
rs957816	0.82[CEU][hapmap]
rs9886561	1.00[CEU][hapmap];1.00[JPT][hapmap];0.84[AMR][1000 genomes];0.93[EUR][1000 genomes];0.91[ASN][1000 genomes]
rs9987099	0.95[CEU][hapmap];1.00[JPT][hapmap];0.84[EUR][1000 genomes];0.91[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	esv3481417	chr8:85279453-86145229	Active TSS Weak transcription Flanking Active TSS Enhancers Strong transcription Bivalent Enhancer Transcr. at gene 5' and 3' ZNF genes & repeats Bivalent/Poised TSS Genic enhancers Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	29 gene(s)	inside rSNPs	diseases
2	esv3481418	chr8:85279453-86145229	Enhancers Weak transcription Active TSS Flanking Active TSS Strong transcription Flanking Bivalent TSS/Enh ZNF genes & repeats Genic enhancers Bivalent Enhancer Transcr. at gene 5' and 3' Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	29 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	chr8:85482800-85490200	Weak transcription	Pancreas	Pancrea

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