Variant report

Variant	rs2822943
Chromosome Location	chr21:16190208-16190209
allele	A/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 52 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:51)

rs_ID	r²[population]
rs1041402	0.89[CEU][hapmap];1.00[YRI][hapmap];0.93[EUR][1000 genomes]
rs10482860	1.00[CEU][hapmap];1.00[YRI][hapmap];0.92[EUR][1000 genomes]
rs13047105	1.00[AFR][1000 genomes];0.92[EUR][1000 genomes]
rs13047199	1.00[CEU][hapmap];1.00[YRI][hapmap];0.92[AMR][1000 genomes];0.96[EUR][1000 genomes]
rs13048782	0.88[CEU][hapmap]
rs13051727	0.89[CEU][hapmap];0.83[CHB][hapmap];1.00[JPT][hapmap];1.00[AFR][1000 genomes];0.98[AMR][1000 genomes];0.96[EUR][1000 genomes];0.90[ASN][1000 genomes]
rs13052243	1.00[CEU][hapmap];1.00[JPT][hapmap];1.00[YRI][hapmap]
rs13433511	0.95[AMR][1000 genomes];0.96[EUR][1000 genomes];0.90[ASN][1000 genomes]
rs1569338	1.00[JPT][hapmap];0.90[ASN][1000 genomes]
rs17241011	0.84[JPT][hapmap];0.84[ASN][1000 genomes]
rs17274666	1.00[YRI][hapmap]
rs17306721	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];0.91[ASN][1000 genomes]
rs1964922	1.00[AFR][1000 genomes];0.93[EUR][1000 genomes]
rs1964923	1.00[AFR][1000 genomes];0.93[EUR][1000 genomes]
rs2178898	1.00[YRI][hapmap]
rs2822930	1.00[CEU][hapmap];1.00[YRI][hapmap]
rs2822934	1.00[CEU][hapmap];1.00[YRI][hapmap]
rs2822935	1.00[YRI][hapmap]
rs2822936	0.84[CHB][hapmap];1.00[JPT][hapmap]
rs2822939	1.00[JPT][hapmap];0.89[ASN][1000 genomes]
rs2822941	1.00[JPT][hapmap];0.89[ASN][1000 genomes]
rs2822942	1.00[CEU][hapmap];0.83[CHB][hapmap];1.00[JPT][hapmap];1.00[YRI][hapmap];1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];0.99[EUR][1000 genomes];0.91[ASN][1000 genomes]
rs2822944	1.00[CEU][hapmap];0.83[CHB][hapmap];1.00[JPT][hapmap];1.00[YRI][hapmap];1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];0.91[ASN][1000 genomes]
rs2822945	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];0.91[ASN][1000 genomes]
rs2822948	1.00[CEU][hapmap];0.84[JPT][hapmap];1.00[YRI][hapmap];0.98[AMR][1000 genomes];0.98[EUR][1000 genomes];0.83[ASN][1000 genomes]
rs2822949	1.00[CEU][hapmap];0.84[JPT][hapmap];1.00[YRI][hapmap];1.00[AFR][1000 genomes];0.98[AMR][1000 genomes];0.98[EUR][1000 genomes];0.81[ASN][1000 genomes]
rs2822950	1.00[CEU][hapmap];0.98[AMR][1000 genomes];0.97[EUR][1000 genomes]
rs2822951	1.00[CEU][hapmap];0.88[JPT][hapmap];0.98[AMR][1000 genomes];0.98[EUR][1000 genomes];0.83[ASN][1000 genomes]
rs2822954	0.84[JPT][hapmap];1.00[YRI][hapmap];1.00[AFR][1000 genomes];0.94[AMR][1000 genomes];0.97[EUR][1000 genomes];0.84[ASN][1000 genomes]
rs2822955	0.84[JPT][hapmap];0.82[ASN][1000 genomes]
rs2822956	1.00[CEU][hapmap];0.91[EUR][1000 genomes]
rs2822959	0.80[CEU][hapmap]
rs28385576	1.00[AFR][1000 genomes];0.95[EUR][1000 genomes]
rs34031799	0.92[AMR][1000 genomes];0.96[EUR][1000 genomes]
rs34189799	1.00[AFR][1000 genomes];0.95[EUR][1000 genomes]
rs34352557	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];0.91[ASN][1000 genomes]
rs34424808	1.00[AFR][1000 genomes];0.92[EUR][1000 genomes]
rs34989434	0.94[AMR][1000 genomes];0.96[EUR][1000 genomes]
rs35408407	1.00[AFR][1000 genomes];0.82[EUR][1000 genomes]
rs35937945	1.00[AFR][1000 genomes];0.98[AMR][1000 genomes];0.96[EUR][1000 genomes];0.88[ASN][1000 genomes]
rs57323609	0.84[ASN][1000 genomes]
rs57530452	0.89[ASN][1000 genomes]
rs59113791	0.84[ASN][1000 genomes]
rs61161554	0.84[ASN][1000 genomes]
rs62219731	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];0.98[EUR][1000 genomes];0.89[ASN][1000 genomes]
rs62219732	0.87[AFR][1000 genomes];0.98[AMR][1000 genomes];1.00[EUR][1000 genomes];0.91[ASN][1000 genomes]
rs62219736	0.86[AFR][1000 genomes];0.92[EUR][1000 genomes]
rs62219737	0.88[AMR][1000 genomes];0.95[EUR][1000 genomes]
rs7277621	0.80[CEU][hapmap];0.84[JPT][hapmap];0.84[ASN][1000 genomes]
rs7281621	0.80[CEU][hapmap];0.84[JPT][hapmap];0.82[AMR][1000 genomes];0.84[ASN][1000 genomes]
rs9979051	0.84[CHB][hapmap];1.00[JPT][hapmap]

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

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv869911	chr21:16184645-16210579	Enhancers Weak transcription Flanking Active TSS	TF binding region Chromatin interactive region lncRNA	2 gene(s)	inside rSNPs	n/a

No data

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

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr21:16189600-16190600	Enhancers	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell

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