Variant report

Variant	rs7279043
Chromosome Location	chr21:18021716-18021717
allele	C/T
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 46 )
Associated
traits (count: 2 )

rSNPs within LD-proxies of this variant (count:43)

rs_ID	r²[population]
rs11088586	0.94[AMR][1000 genomes];0.91[EUR][1000 genomes]
rs1116415	0.96[AMR][1000 genomes];0.99[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs1129247	0.92[AMR][1000 genomes];0.99[EUR][1000 genomes]
rs11702837	0.97[EUR][1000 genomes]
rs12626359	0.94[AMR][1000 genomes];0.91[EUR][1000 genomes]
rs12626360	0.95[AMR][1000 genomes];0.98[EUR][1000 genomes]
rs12627380	0.93[EUR][1000 genomes]
rs12627437	0.94[AMR][1000 genomes];0.91[EUR][1000 genomes]
rs12627532	0.95[AMR][1000 genomes];0.98[EUR][1000 genomes]
rs13050616	0.91[EUR][1000 genomes]
rs13051672	0.97[EUR][1000 genomes]
rs13052472	0.98[EUR][1000 genomes]
rs2027623	0.88[AMR][1000 genomes];0.97[EUR][1000 genomes]
rs2027624	0.95[AMR][1000 genomes];0.98[EUR][1000 genomes]
rs2027625	0.95[AMR][1000 genomes];0.98[EUR][1000 genomes]
rs2154727	0.95[AMR][1000 genomes];0.99[EUR][1000 genomes]
rs2211987	0.95[AMR][1000 genomes];0.99[EUR][1000 genomes]
rs2211988	0.95[AMR][1000 genomes];0.99[EUR][1000 genomes]
rs2211990	0.95[AMR][1000 genomes];0.99[EUR][1000 genomes]
rs2823929	0.95[AMR][1000 genomes];0.98[EUR][1000 genomes]
rs2823930	0.95[AMR][1000 genomes];0.98[EUR][1000 genomes]
rs2823931	0.95[AMR][1000 genomes];0.98[EUR][1000 genomes]
rs2823932	0.92[AMR][1000 genomes];0.99[EUR][1000 genomes]
rs2823933	0.96[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs2823959	0.82[AMR][1000 genomes];0.80[EUR][1000 genomes];0.83[ASN][1000 genomes]
rs2823960	0.82[AMR][1000 genomes];0.80[EUR][1000 genomes];0.85[ASN][1000 genomes]
rs2823961	0.82[AMR][1000 genomes];0.80[EUR][1000 genomes];0.85[ASN][1000 genomes]
rs2823962	0.82[AMR][1000 genomes];0.80[EUR][1000 genomes];0.84[ASN][1000 genomes]
rs2823963	0.82[AMR][1000 genomes];0.84[ASN][1000 genomes]
rs2823964	0.83[ASN][1000 genomes]
rs2823965	0.83[ASN][1000 genomes]
rs4485639	0.96[AMR][1000 genomes];0.99[EUR][1000 genomes];0.92[ASN][1000 genomes]
rs4485640	0.95[AMR][1000 genomes];0.99[EUR][1000 genomes]
rs7277443	0.82[AMR][1000 genomes];0.80[EUR][1000 genomes];0.85[ASN][1000 genomes]
rs7281422	0.82[AMR][1000 genomes];0.80[EUR][1000 genomes];0.84[ASN][1000 genomes]
rs8133801	0.96[AMR][1000 genomes];0.99[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs8134854	0.96[AMR][1000 genomes];0.98[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs9637008	0.98[EUR][1000 genomes]
rs9784203	0.81[AMR][1000 genomes];0.80[EUR][1000 genomes];0.85[ASN][1000 genomes]
rs9974183	0.83[ASN][1000 genomes]
rs9980343	0.91[EUR][1000 genomes]
rs9984100	0.95[AMR][1000 genomes];0.98[EUR][1000 genomes]
rs9984105	0.95[AMR][1000 genomes];0.98[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	nsv1064857	chr21:17628760-18533131	Enhancers Active TSS Weak transcription ZNF genes & repeats Flanking Active TSS Strong transcription Bivalent/Poised TSS Bivalent Enhancer Genic enhancers Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA miRNA	345 gene(s)	inside rSNPs	diseases
2	nsv544382	chr21:17628760-18533131	Active TSS Enhancers Weak transcription Flanking Active TSS Strong transcription ZNF genes & repeats Genic enhancers Bivalent Enhancer Bivalent/Poised TSS Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA miRNA	345 gene(s)	inside rSNPs	diseases
3	nsv834052	chr21:17967385-18142224	Strong transcription Flanking Active TSS Enhancers Weak transcription Genic enhancers Active TSS ZNF genes & repeats	TF binding region Chromatin interactive region lncRNA	17 gene(s)	inside rSNPs	diseases

mRNA abundance (count:2)

SNP	Gene	Cis/trans	Tissue	Source
rs7279043	AP000473.8	cis	Thyroid	GTEx
rs7279043	AP000473.8	cis	Nerve Tibial	GTEx

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

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr21:18021400-18022400	Weak transcription	Fetal Stomach	stomach
2	chr21:18021600-18022800	Enhancers	Fetal Brain Male	brain

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