Variant report

Variant	rs16882626
Chromosome Location	chr6:73314929-73314930
allele	A/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 46 )
Associated
traits (count: 0)

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

rs_ID	r²[population]
rs1112877	1.00[EUR][1000 genomes]
rs16882541	1.00[EUR][1000 genomes]
rs16882560	1.00[EUR][1000 genomes]
rs16882652	0.88[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs4088773	1.00[EUR][1000 genomes]
rs55676608	0.83[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs55817542	1.00[EUR][1000 genomes]
rs55885580	1.00[EUR][1000 genomes]
rs56173098	0.83[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs58136138	1.00[EUR][1000 genomes]
rs59070352	0.83[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs59119615	1.00[EUR][1000 genomes]
rs59508897	1.00[EUR][1000 genomes]
rs60830036	1.00[EUR][1000 genomes]
rs60941898	1.00[EUR][1000 genomes]
rs61530646	1.00[EUR][1000 genomes]
rs6453590	1.00[EUR][1000 genomes]
rs6907438	1.00[EUR][1000 genomes]
rs6917358	1.00[EUR][1000 genomes]
rs6929554	1.00[EUR][1000 genomes]
rs6931019	1.00[EUR][1000 genomes]
rs73751720	0.83[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs73751722	1.00[EUR][1000 genomes]
rs73751723	1.00[EUR][1000 genomes]
rs73751728	1.00[EUR][1000 genomes]
rs73751730	1.00[EUR][1000 genomes]
rs73751731	0.83[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs73751732	1.00[EUR][1000 genomes]
rs73751734	1.00[EUR][1000 genomes]
rs73753349	1.00[EUR][1000 genomes]
rs73753351	1.00[EUR][1000 genomes]
rs73753353	1.00[EUR][1000 genomes]
rs73753354	1.00[EUR][1000 genomes]
rs73753355	1.00[EUR][1000 genomes]
rs73753357	0.83[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs73753358	0.83[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs73753363	1.00[EUR][1000 genomes]
rs73754703	0.83[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs7754398	1.00[EUR][1000 genomes]
rs7757187	1.00[EUR][1000 genomes]
rs7757848	1.00[EUR][1000 genomes]
rs7773525	1.00[EUR][1000 genomes]
rs7774395	1.00[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	nsv1023809	chr6:73157813-73477997	Bivalent Enhancer Weak transcription Flanking Bivalent TSS/Enh Enhancers Active TSS ZNF genes & repeats Flanking Active TSS Strong transcription Bivalent/Poised TSS Genic enhancers	TF binding region CpG island Chromatin interactive region lncRNA	4 gene(s)	inside rSNPs	diseases
2	nsv538303	chr6:73157813-73477997	Active TSS Weak transcription Enhancers Strong transcription Flanking Active TSS Bivalent/Poised TSS Flanking Bivalent TSS/Enh Bivalent Enhancer ZNF genes & repeats Genic enhancers	TF binding region CpG island Chromatin interactive region lncRNA	4 gene(s)	inside rSNPs	diseases
3	esv3347486	chr6:73283590-73445976	Enhancers Active TSS Flanking Active TSS Flanking Bivalent TSS/Enh Weak transcription Bivalent Enhancer Bivalent/Poised TSS Strong transcription ZNF genes & repeats Genic enhancers	TF binding region CpG island Chromatin interactive region lncRNA	4 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	chr6:73314800-73316200	Enhancers	Fetal Heart	heart

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