Variant report

Variant	rs3853262
Chromosome Location	chr8:114118556-114118557
allele	A/T
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 126 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:119)

rs_ID	r²[population]
rs10092868	0.96[CEU][hapmap]
rs10094486	0.89[AFR][1000 genomes];0.90[AMR][1000 genomes];0.91[EUR][1000 genomes];0.93[ASN][1000 genomes]
rs10108312	0.96[CEU][hapmap]
rs1014321	0.96[CEU][hapmap]
rs1017829	1.00[CEU][hapmap]
rs1021876	0.96[CEU][hapmap]
rs1021877	0.96[CEU][hapmap]
rs1021878	0.96[CEU][hapmap]
rs1038192	0.96[CEU][hapmap]
rs10955642	0.90[AMR][1000 genomes];0.91[EUR][1000 genomes];0.93[ASN][1000 genomes]
rs10955646	0.96[CEU][hapmap]
rs11985196	0.91[AFR][1000 genomes];0.92[AMR][1000 genomes];0.92[EUR][1000 genomes];0.93[ASN][1000 genomes]
rs11990304	0.93[CEU][hapmap]
rs12541577	1.00[CEU][hapmap]
rs12550692	0.96[CEU][hapmap]
rs12675949	1.00[CEU][hapmap]
rs13270413	0.89[CEU][hapmap]
rs1351388	1.00[CEU][hapmap]
rs1351389	0.96[CEU][hapmap]
rs1351392	0.96[CEU][hapmap]
rs1354445	0.96[AFR][1000 genomes];0.94[AMR][1000 genomes];0.99[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs1354446	0.96[CEU][hapmap];0.96[AFR][1000 genomes];0.94[AMR][1000 genomes];0.96[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs1383293	0.96[CEU][hapmap]
rs1383294	0.96[CEU][hapmap]
rs1383296	0.96[CEU][hapmap]
rs1383298	0.96[CEU][hapmap];0.94[AFR][1000 genomes];0.92[AMR][1000 genomes];0.91[EUR][1000 genomes];0.93[ASN][1000 genomes]
rs1383300	0.96[CEU][hapmap]
rs1394268	0.96[AFR][1000 genomes];0.93[AMR][1000 genomes];0.94[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs1394269	0.96[CEU][hapmap];0.92[AFR][1000 genomes];0.94[AMR][1000 genomes];0.95[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs1394270	0.96[CEU][hapmap]
rs1394271	0.96[CEU][hapmap]
rs1402943	0.89[CEU][hapmap]
rs1472723	0.92[AFR][1000 genomes];0.94[AMR][1000 genomes];0.96[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs1472724	0.96[CEU][hapmap]
rs1480443	0.97[ASN][1000 genomes]
rs1480446	0.96[CEU][hapmap]
rs1480448	0.96[CEU][hapmap]
rs1480455	0.96[CEU][hapmap]
rs1480462	1.00[CEU][hapmap]
rs1480463	0.96[CEU][hapmap]
rs1504337	0.93[ASN][1000 genomes]
rs1504340	0.88[AMR][1000 genomes];0.90[EUR][1000 genomes];0.93[ASN][1000 genomes]
rs1504341	0.96[CEU][hapmap]
rs1504347	0.96[CEU][hapmap]
rs1522057	1.00[CEU][hapmap]
rs1522058	0.89[CEU][hapmap]
rs1522064	1.00[CEU][hapmap]
rs1522065	0.89[CEU][hapmap];0.81[AMR][1000 genomes];0.90[EUR][1000 genomes];0.93[ASN][1000 genomes]
rs1566835	0.96[CEU][hapmap]
rs17602393	0.96[CEU][hapmap]
rs17605667	1.00[CEU][hapmap]
rs17607120	0.93[CEU][hapmap]
rs1817453	0.96[CEU][hapmap]
rs1827626	0.87[AFR][1000 genomes];0.93[AMR][1000 genomes];0.95[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs1857718	0.96[CEU][hapmap]
rs1904217	0.81[ASN][1000 genomes]
rs1904218	0.82[EUR][1000 genomes];0.81[ASN][1000 genomes]
rs1969113	0.96[CEU][hapmap]
rs2030506	0.92[CEU][hapmap]
rs2030507	0.92[CEU][hapmap]
rs2127689	0.96[CEU][hapmap]
rs2134839	0.96[CEU][hapmap]
rs2134840	0.96[CEU][hapmap]
rs2134842	0.96[CEU][hapmap]
rs2356050	0.89[CEU][hapmap]
rs2356203	0.89[CEU][hapmap]
rs2356204	0.89[CEU][hapmap]
rs2883875	1.00[CEU][hapmap]
rs3853260	1.00[CEU][hapmap];0.96[AFR][1000 genomes];0.94[AMR][1000 genomes];0.99[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs3853261	1.00[CEU][hapmap];0.96[AFR][1000 genomes];0.94[AMR][1000 genomes];0.99[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs3912243	1.00[CEU][hapmap];0.92[AFR][1000 genomes];0.94[AMR][1000 genomes];0.99[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs4242551	1.00[CEU][hapmap]
rs4437684	1.00[CEU][hapmap]
rs4509361	0.96[CEU][hapmap]
rs4565484	0.88[CEU][hapmap]
rs4876300	0.96[CEU][hapmap]
rs58021089	0.89[AFR][1000 genomes];0.90[AMR][1000 genomes];0.91[EUR][1000 genomes];0.93[ASN][1000 genomes]
rs6469452	1.00[CEU][hapmap]
rs6982602	0.96[CEU][hapmap]
rs6995484	0.96[CEU][hapmap]
rs6999773	0.84[AFR][1000 genomes];0.90[AMR][1000 genomes];0.90[EUR][1000 genomes];0.93[ASN][1000 genomes]
rs6999828	0.96[CEU][hapmap];0.94[AMR][1000 genomes];0.96[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs7004426	0.84[ASN][1000 genomes]
rs7007093	0.96[CEU][hapmap]
rs7007990	0.96[CEU][hapmap];0.89[AMR][1000 genomes];0.81[EUR][1000 genomes];0.81[ASN][1000 genomes]
rs7013894	0.96[CEU][hapmap]
rs7014643	0.96[CEU][hapmap]
rs7015519	0.96[CEU][hapmap]
rs7015794	0.96[CEU][hapmap]
rs7812581	0.96[CEU][hapmap]
rs7812971	0.97[ASN][1000 genomes]
rs7817385	0.96[AFR][1000 genomes];0.92[AMR][1000 genomes];0.92[EUR][1000 genomes];0.93[ASN][1000 genomes]
rs7817505	0.96[CEU][hapmap];0.96[AFR][1000 genomes];0.92[AMR][1000 genomes];0.92[EUR][1000 genomes];0.93[ASN][1000 genomes]
rs7820383	0.96[CEU][hapmap];0.88[AMR][1000 genomes];0.90[EUR][1000 genomes];0.93[ASN][1000 genomes]
rs7821294	0.96[CEU][hapmap]
rs7824290	1.00[CEU][hapmap]
rs7824314	0.96[CEU][hapmap];0.96[AFR][1000 genomes];0.92[AMR][1000 genomes];0.91[EUR][1000 genomes];0.93[ASN][1000 genomes]
rs7824563	0.96[AFR][1000 genomes];0.92[AMR][1000 genomes];0.91[EUR][1000 genomes];0.93[ASN][1000 genomes]
rs7824652	0.96[CEU][hapmap]
rs7825515	0.89[CEU][hapmap]
rs7828518	1.00[CEU][hapmap]
rs7829709	0.96[CEU][hapmap]
rs7829954	0.96[CEU][hapmap]
rs7833634	0.96[CEU][hapmap];0.81[AMR][1000 genomes];0.92[EUR][1000 genomes];0.93[ASN][1000 genomes]
rs7834106	1.00[CEU][hapmap]
rs7834141	0.85[CEU][hapmap]
rs7835368	1.00[CEU][hapmap];0.94[AMR][1000 genomes];0.97[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs7836578	0.96[CEU][hapmap]
rs7840572	0.96[CEU][hapmap]
rs7840935	0.96[CEU][hapmap]
rs899831	0.96[CEU][hapmap]
rs9283946	0.96[CEU][hapmap]
rs9297488	0.96[CEU][hapmap]
rs9642818	1.00[CEU][hapmap]
rs971124	0.96[CEU][hapmap]
rs979895	0.96[CEU][hapmap]
rs979896	0.96[CEU][hapmap]
rs990220	0.96[CEU][hapmap]
rs996252	0.96[CEU][hapmap]

Variant overlapped rSNPs/rCNVs (count:7 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	esv2753595	chr8:113283214-114190390	Enhancers Weak transcription Active TSS Strong transcription Bivalent Enhancer Flanking Active TSS ZNF genes & repeats Flanking Bivalent TSS/Enh Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA	6 gene(s)	inside rSNPs	diseases
2	esv2753160	chr8:113920441-114190390	Enhancers Flanking Active TSS Weak transcription ZNF genes & repeats Active TSS	TF binding region CpG island Chromatin interactive region	1 gene(s)	inside rSNPs	diseases
3	nsv534557	chr8:113929740-114131155	Enhancers Active TSS ZNF genes & repeats Weak transcription Flanking Active TSS	Chromatin interactive region	n/a	inside rSNPs	diseases
4	esv2756532	chr8:113931884-114120265	Enhancers Weak transcription Flanking Active TSS Active TSS	Chromatin interactive region	n/a	inside rSNPs	diseases
5	esv2754581	chr8:114029421-114419106	Weak transcription Enhancers Active TSS Flanking Active TSS ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA	2 gene(s)	inside rSNPs	diseases
6	nsv831428	chr8:114102983-114320802	Enhancers Weak transcription Flanking Active TSS Active TSS ZNF genes & repeats	TF binding region CpG island Chromatin interactive region	1 gene(s)	inside rSNPs	diseases
7	nsv916637	chr8:114116303-114338450	Weak transcription Enhancers Active TSS Flanking Active TSS ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA	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	chr8:114118000-114118800	Enhancers	HUVEC	blood vessel

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