Variant report

Variant	rs9979924
Chromosome Location	chr21:18021052-18021053
allele	G/T
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 21 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:18)

rs_ID	r²[population]
rs11910784	1.00[EUR][1000 genomes]
rs17000801	1.00[EUR][1000 genomes]
rs2243706	0.83[ASN][1000 genomes]
rs2823927	1.00[JPT][hapmap];0.94[ASN][1000 genomes]
rs2823928	0.82[EUR][1000 genomes];0.94[ASN][1000 genomes]
rs2823935	0.83[AFR][1000 genomes]
rs2896764	0.94[ASN][1000 genomes]
rs72631903	1.00[EUR][1000 genomes]
rs73891646	0.89[EUR][1000 genomes]
rs8127374	0.90[EUR][1000 genomes]
rs8128579	0.90[EUR][1000 genomes]
rs8131576	0.90[EUR][1000 genomes]
rs8132734	0.90[EUR][1000 genomes]
rs980067	1.00[JPT][hapmap];1.00[EUR][1000 genomes];0.94[ASN][1000 genomes]
rs9974489	0.81[AMR][1000 genomes]
rs9975821	0.90[EUR][1000 genomes]
rs9976375	0.90[EUR][1000 genomes]
rs9980923	0.81[AMR][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

No data

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

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr21:18019400-18021600	Weak transcription	Fetal Brain Male	brain

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dbSNP/dbVar ID: rs12345 /nsv7879
a single nucleotide as 0-based coordinates: chr1:12345
chromosomal regions: chr1:12345-34567

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