Variant report

Variant	rs28404770
Chromosome Location	chr21:27973835-27973836
allele	A/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 45 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:42)

rs_ID	r²[population]
rs13433470	0.81[AFR][1000 genomes]
rs1543775	0.87[AFR][1000 genomes]
rs1893573	0.90[AFR][1000 genomes]
rs1893576	0.84[AMR][1000 genomes];0.93[EUR][1000 genomes]
rs2135305	0.90[AFR][1000 genomes]
rs2830293	0.84[AMR][1000 genomes];0.90[EUR][1000 genomes]
rs2830294	0.84[AMR][1000 genomes];0.93[EUR][1000 genomes]
rs2830295	0.95[AFR][1000 genomes]
rs2830296	0.96[AFR][1000 genomes]
rs2830298	0.97[AFR][1000 genomes]
rs2830299	0.97[AFR][1000 genomes]
rs2830300	0.98[AFR][1000 genomes]
rs2830301	0.98[AFR][1000 genomes]
rs28401356	0.97[AFR][1000 genomes]
rs28525622	0.90[AFR][1000 genomes]
rs28678819	0.91[AFR][1000 genomes]
rs57795228	1.00[EUR][1000 genomes]
rs59317497	0.84[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs73351190	0.81[AFR][1000 genomes]
rs73353008	0.86[AFR][1000 genomes]
rs73898272	0.93[EUR][1000 genomes]
rs73898279	0.93[EUR][1000 genomes]
rs73898281	0.93[EUR][1000 genomes]
rs73898282	0.93[EUR][1000 genomes]
rs73898283	1.00[EUR][1000 genomes]
rs8128643	0.93[EUR][1000 genomes]
rs8129932	0.86[AFR][1000 genomes]
rs8129933	0.83[AFR][1000 genomes]
rs8133538	0.83[AFR][1000 genomes]
rs9974221	0.90[AFR][1000 genomes]
rs9975467	0.90[AFR][1000 genomes]
rs9975732	0.84[AFR][1000 genomes]
rs9977977	0.84[AMR][1000 genomes];0.93[EUR][1000 genomes]
rs9978127	0.90[AFR][1000 genomes]
rs9979121	0.99[AFR][1000 genomes];0.95[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs9979840	0.95[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs9979986	0.95[AFR][1000 genomes]
rs9980194	0.96[AFR][1000 genomes]
rs9980300	0.91[EUR][1000 genomes]
rs9980419	0.95[AFR][1000 genomes]
rs9984233	0.93[EUR][1000 genomes]
rs9984431	0.93[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	nsv1056506	chr21:27332898-28049880	Weak transcription Enhancers Strong transcription Flanking Active TSS Genic enhancers ZNF genes & repeats Active TSS Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3' Bivalent/Poised TSS Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	25 gene(s)	inside rSNPs	diseases
2	nsv544412	chr21:27332898-28049880	Weak transcription Flanking Active TSS Strong transcription Enhancers Genic enhancers Bivalent/Poised TSS ZNF genes & repeats Active TSS Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	25 gene(s)	inside rSNPs	diseases
3	nsv544413	chr21:27942060-28065995	Active TSS Weak transcription Enhancers Bivalent/Poised TSS Flanking Active TSS Flanking Bivalent TSS/Enh ZNF genes & repeats Bivalent Enhancer Transcr. at gene 5' and 3' Strong transcription	TF binding region CpG island Chromatin interactive region lncRNA	1 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	chr21:27973200-27974000	Weak transcription	Dnd41	blood

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