Variant report

Variant	rs28678819
Chromosome Location	chr21:27959351-27959352
allele	A/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 43 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:40)

rs_ID	r²[population]
rs13433470	0.89[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs1543775	0.96[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs1893573	0.97[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs2135305	0.99[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs2830275	0.81[AFR][1000 genomes];0.83[AMR][1000 genomes]
rs2830280	0.84[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs2830282	1.00[AMR][1000 genomes]
rs2830295	0.92[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs2830296	0.93[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs2830298	0.92[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs2830299	0.92[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs2830300	0.91[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs2830301	0.91[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs28401356	0.92[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs28404770	0.91[AFR][1000 genomes]
rs28525622	0.99[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs28572488	0.83[AMR][1000 genomes]
rs28624518	0.83[AMR][1000 genomes]
rs57821067	1.00[AMR][1000 genomes]
rs7277524	0.87[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs7283190	0.86[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs73351185	1.00[AMR][1000 genomes]
rs73351190	0.89[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs73353008	0.95[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs8127446	0.83[AMR][1000 genomes]
rs8128689	0.87[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs8129932	0.94[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs8129933	0.91[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs8130654	0.88[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs8133538	0.91[AFR][1000 genomes];0.91[AMR][1000 genomes]
rs9974221	0.99[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs9975467	0.99[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs9975732	0.92[AFR][1000 genomes];0.91[AMR][1000 genomes]
rs9978127	0.99[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs9979121	0.90[AFR][1000 genomes]
rs9979986	0.92[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs9980194	0.93[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs9980419	0.92[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs9984233	0.86[AFR][1000 genomes]
rs9989934	0.87[AFR][1000 genomes];1.00[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	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:2 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr21:27957200-27959600	Weak transcription	NHDF-Ad	bronchial
2	chr21:27958400-27962200	Enhancers	Fetal Adrenal Gland	Adrenal Gland

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