Variant report

Variant	rs72684567
Chromosome Location	chr4:120864483-120864484
allele	C/T
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 49 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:47)

rs_ID	r²[population]
rs11098544	0.81[EUR][1000 genomes]
rs2304801	0.81[EUR][1000 genomes]
rs55754134	0.88[EUR][1000 genomes]
rs56036619	0.81[EUR][1000 genomes]
rs56038013	0.81[EUR][1000 genomes]
rs56042330	1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs56234746	0.81[EUR][1000 genomes]
rs72682827	0.81[EUR][1000 genomes]
rs72682828	0.81[EUR][1000 genomes]
rs72682832	0.81[EUR][1000 genomes]
rs72682843	0.81[EUR][1000 genomes]
rs72682844	0.81[EUR][1000 genomes]
rs72682845	1.00[AMR][1000 genomes];0.81[EUR][1000 genomes]
rs72682877	0.81[EUR][1000 genomes]
rs72682885	0.81[EUR][1000 genomes]
rs72682891	0.81[EUR][1000 genomes]
rs72682897	1.00[AMR][1000 genomes];0.81[EUR][1000 genomes]
rs72682898	0.81[EUR][1000 genomes]
rs72682901	1.00[AMR][1000 genomes];0.81[EUR][1000 genomes]
rs72682902	0.81[EUR][1000 genomes]
rs72684508	0.81[EUR][1000 genomes]
rs72684509	1.00[AMR][1000 genomes];0.81[EUR][1000 genomes]
rs72684511	0.81[EUR][1000 genomes]
rs72684514	1.00[AMR][1000 genomes];0.81[EUR][1000 genomes]
rs72684533	0.87[EUR][1000 genomes]
rs72684534	0.87[EUR][1000 genomes]
rs72684540	0.88[EUR][1000 genomes]
rs72684541	0.88[EUR][1000 genomes]
rs72684560	0.88[EUR][1000 genomes]
rs72684562	0.88[EUR][1000 genomes]
rs72684564	0.88[EUR][1000 genomes]
rs72684570	1.00[EUR][1000 genomes]
rs72684581	1.00[EUR][1000 genomes]
rs72684584	1.00[EUR][1000 genomes]
rs72684587	1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs72684588	1.00[AMR][1000 genomes];0.81[EUR][1000 genomes]
rs72684589	1.00[AMR][1000 genomes];0.81[EUR][1000 genomes]
rs72684590	0.81[EUR][1000 genomes]
rs72684591	1.00[AMR][1000 genomes];0.81[EUR][1000 genomes]
rs72684592	1.00[AMR][1000 genomes];0.81[EUR][1000 genomes]
rs72684593	1.00[AMR][1000 genomes];0.81[EUR][1000 genomes]
rs72684594	1.00[AMR][1000 genomes]
rs72684595	1.00[AMR][1000 genomes];0.81[EUR][1000 genomes]
rs72684596	1.00[AMR][1000 genomes];0.81[EUR][1000 genomes]
rs72684597	1.00[AMR][1000 genomes];0.81[EUR][1000 genomes]
rs72684599	1.00[AMR][1000 genomes];0.81[EUR][1000 genomes]
rs72684600	0.81[EUR][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:2 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv532739	chr4:120392824-121098103	Enhancers Flanking Active TSS Strong transcription Weak transcription Bivalent/Poised TSS Active TSS ZNF genes & repeats Bivalent Enhancer Genic enhancers Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	33 gene(s)	inside rSNPs	diseases
2	nsv879849	chr4:120823634-120922444	Strong transcription Enhancers Active TSS Flanking Active TSS Transcr. at gene 5' and 3' Weak transcription Genic enhancers	TF binding region CpG island Chromatin interactive region lncRNA	3 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	chr4:120864000-120865200	Enhancers	Fetal Heart	heart

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