Variant report

Variant	rs473351
Chromosome Location	chr2:169779896-169779897
allele	A/C/G/T
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 57 )
Associated
traits (count: 1 )

rSNPs within LD-proxies of this variant (count:54)

rs_ID	r²[population]
rs1101531	0.80[EUR][1000 genomes]
rs1101533	0.92[CEU][hapmap];0.80[EUR][1000 genomes]
rs1101534	0.81[EUR][1000 genomes]
rs1581397	0.96[CEU][hapmap];0.89[TSI][hapmap];0.88[EUR][1000 genomes]
rs2250677	0.85[EUR][1000 genomes]
rs2544360	0.84[EUR][1000 genomes]
rs2544367	0.96[CEU][hapmap];0.87[TSI][hapmap];0.88[EUR][1000 genomes]
rs2685803	0.96[CEU][hapmap];0.88[EUR][1000 genomes]
rs2685804	0.88[EUR][1000 genomes]
rs2685805	0.96[CEU][hapmap];0.87[TSI][hapmap];0.88[EUR][1000 genomes]
rs2685806	0.88[EUR][1000 genomes]
rs2685807	0.85[EUR][1000 genomes]
rs2685808	0.87[EUR][1000 genomes]
rs2685810	0.88[EUR][1000 genomes]
rs2685811	0.88[EUR][1000 genomes]
rs2685812	0.96[CEU][hapmap];0.89[TSI][hapmap];0.88[EUR][1000 genomes]
rs2685813	0.96[CEU][hapmap];0.84[TSI][hapmap];0.88[EUR][1000 genomes]
rs2685814	0.89[CEU][hapmap];0.87[TSI][hapmap];0.88[EUR][1000 genomes]
rs2947987	0.86[EUR][1000 genomes]
rs472614	0.90[EUR][1000 genomes]
rs478333	0.90[EUR][1000 genomes]
rs479682	0.96[CEU][hapmap];0.89[TSI][hapmap];0.89[EUR][1000 genomes]
rs480562	0.96[CEU][hapmap];0.89[EUR][1000 genomes]
rs482508	0.89[EUR][1000 genomes]
rs495714	0.91[EUR][1000 genomes]
rs496550	0.91[EUR][1000 genomes]
rs497692	0.90[EUR][1000 genomes]
rs500432	0.86[AMR][1000 genomes];0.91[EUR][1000 genomes];0.88[ASN][1000 genomes]
rs503931	0.91[EUR][1000 genomes]
rs519035	0.91[EUR][1000 genomes]
rs519887	0.91[EUR][1000 genomes]
rs527150	0.91[EUR][1000 genomes]
rs531772	0.90[AFR][1000 genomes];0.95[AMR][1000 genomes];0.99[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs551754	0.91[EUR][1000 genomes]
rs555975	0.89[EUR][1000 genomes]
rs565412	0.96[CEU][hapmap];0.89[TSI][hapmap];0.89[EUR][1000 genomes]
rs567074	0.92[CEU][hapmap];0.84[TSI][hapmap];0.86[EUR][1000 genomes]
rs575671	0.98[AMR][1000 genomes];0.99[EUR][1000 genomes]
rs579275	0.91[EUR][1000 genomes]
rs853772	0.82[CEU][hapmap]
rs853776	0.92[CEU][hapmap];0.85[TSI][hapmap];0.80[EUR][1000 genomes]
rs853778	0.88[CEU][hapmap];0.85[TSI][hapmap]
rs853779	0.92[CEU][hapmap];0.85[TSI][hapmap];0.81[EUR][1000 genomes]
rs853780	0.92[CEU][hapmap];0.83[TSI][hapmap];0.80[EUR][1000 genomes]
rs853781	0.88[CEU][hapmap]
rs853783	0.92[CEU][hapmap];0.85[TSI][hapmap];0.81[EUR][1000 genomes]
rs853784	0.92[CEU][hapmap];0.85[TSI][hapmap];0.81[EUR][1000 genomes]
rs853785	0.96[CEU][hapmap];0.87[TSI][hapmap];0.86[EUR][1000 genomes]
rs853786	0.96[CEU][hapmap];0.87[TSI][hapmap];0.87[EUR][1000 genomes]
rs853788	0.96[CEU][hapmap];0.87[TSI][hapmap];0.87[EUR][1000 genomes]
rs853790	0.83[EUR][1000 genomes]
rs860510	0.96[CEU][hapmap];0.86[EUR][1000 genomes]
rs862662	0.92[CEU][hapmap];0.82[TSI][hapmap];0.83[EUR][1000 genomes]
rs864929	0.80[EUR][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:3 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv583599	chr2:169664227-169903096	Bivalent Enhancer Weak transcription Genic enhancers Strong transcription Enhancers Active TSS Flanking Active TSS ZNF genes & repeats Bivalent/Poised TSS Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	12 gene(s)	inside rSNPs	diseases
2	nsv459943	chr2:169756930-169799010	Bivalent/Poised TSS Enhancers Bivalent Enhancer Flanking Active TSS Weak transcription Flanking Bivalent TSS/Enh Active TSS ZNF genes & repeats Strong transcription Genic enhancers	TF binding region CpG island Chromatin interactive region miRNA target site	4 gene(s)	inside rSNPs	diseases
3	nsv583600	chr2:169756930-169799010	Active TSS Bivalent/Poised TSS Flanking Bivalent TSS/Enh Enhancers Weak transcription Flanking Active TSS Bivalent Enhancer Strong transcription ZNF genes & repeats Genic enhancers	TF binding region CpG island Chromatin interactive region miRNA target site	4 gene(s)	inside rSNPs	diseases

mRNA abundance (count:1)

SNP	Gene	Cis/trans	Tissue	Source
rs473351	AADAT	trans	parietal	SCAN

Chromatin state (count:2 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr2:169776800-169785000	Weak transcription	Fetal Intestine Small	intestine
2	chr2:169778600-169782000	Strong transcription	Liver	Liver

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