Variant report

Variant	rs6853347
Chromosome Location	chr4:106947408-106947409
allele	A/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 65 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:63)

rs_ID	r²[population]
rs10004034	0.90[ASN][1000 genomes]
rs10017707	0.89[ASN][1000 genomes]
rs10155346	1.00[ASN][1000 genomes]
rs10489129	0.93[AFR][1000 genomes];0.89[EUR][1000 genomes]
rs10516530	0.92[ASN][1000 genomes]
rs10516531	0.92[ASN][1000 genomes]
rs11097923	0.90[ASN][1000 genomes]
rs11936196	1.00[ASN][1000 genomes]
rs11938792	0.90[ASN][1000 genomes]
rs11942385	0.93[AFR][1000 genomes];0.89[EUR][1000 genomes]
rs12508029	0.94[ASN][1000 genomes]
rs12512475	0.89[ASN][1000 genomes]
rs17036506	0.93[AFR][1000 genomes];0.89[EUR][1000 genomes]
rs17036511	0.93[AFR][1000 genomes];0.89[EUR][1000 genomes]
rs17036530	0.89[EUR][1000 genomes]
rs17036535	0.89[EUR][1000 genomes]
rs17036581	0.92[ASN][1000 genomes]
rs1988966	1.00[ASN][1000 genomes]
rs2212969	0.90[ASN][1000 genomes]
rs28600991	0.88[ASN][1000 genomes]
rs34305991	0.91[ASN][1000 genomes]
rs34909190	0.89[ASN][1000 genomes]
rs34923623	0.92[ASN][1000 genomes]
rs4264831	0.89[EUR][1000 genomes]
rs4415033	0.88[ASN][1000 genomes]
rs4441824	0.90[ASN][1000 genomes]
rs4472215	0.84[EUR][1000 genomes]
rs4533833	0.89[ASN][1000 genomes]
rs4552462	0.84[EUR][1000 genomes]
rs4560491	0.90[ASN][1000 genomes]
rs4582218	0.91[ASN][1000 genomes]
rs57983950	0.89[ASN][1000 genomes]
rs62320069	0.89[EUR][1000 genomes]
rs62320070	0.89[EUR][1000 genomes]
rs62320112	0.94[AFR][1000 genomes];0.89[EUR][1000 genomes]
rs62320113	0.89[EUR][1000 genomes]
rs62320115	0.93[AFR][1000 genomes];0.89[EUR][1000 genomes]
rs62320116	0.89[EUR][1000 genomes]
rs62320117	0.89[EUR][1000 genomes]
rs62320120	0.89[EUR][1000 genomes]
rs62320124	0.84[EUR][1000 genomes]
rs62320128	0.84[EUR][1000 genomes]
rs62320129	0.84[EUR][1000 genomes]
rs62321364	0.84[EUR][1000 genomes]
rs62321372	0.80[EUR][1000 genomes]
rs62321373	0.80[EUR][1000 genomes]
rs62321374	0.80[EUR][1000 genomes]
rs62321375	0.80[EUR][1000 genomes]
rs62321376	0.80[EUR][1000 genomes]
rs6533241	0.90[ASN][1000 genomes]
rs6533244	0.90[ASN][1000 genomes]
rs67566720	0.91[AFR][1000 genomes];0.89[EUR][1000 genomes]
rs6836796	0.95[ASN][1000 genomes]
rs6848855	0.90[ASN][1000 genomes]
rs72675686	0.89[EUR][1000 genomes]
rs72675692	0.89[EUR][1000 genomes]
rs72675702	0.84[EUR][1000 genomes]
rs72960673	0.95[ASN][1000 genomes]
rs7442226	0.90[ASN][1000 genomes]
rs7677394	0.91[ASN][1000 genomes]
rs7680756	0.90[ASN][1000 genomes]
rs9884121	0.92[ASN][1000 genomes]
rs9993259	0.92[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	nsv1014993	chr4:106796019-106980727	Enhancers Flanking Bivalent TSS/Enh Weak transcription Bivalent/Poised TSS Bivalent Enhancer Strong transcription Active TSS Genic enhancers Flanking Active TSS ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA	9 gene(s)	inside rSNPs	diseases
2	nsv522792	chr4:106895964-106982793	Weak transcription Enhancers Strong transcription ZNF genes & repeats Flanking Active TSS Active TSS Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA	6 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	chr4:106935000-106948400	Weak transcription	Aorta	Aorta

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