Variant report

Variant	rs72881802
Chromosome Location	chr3:61268382-61268383
allele	G/T
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 37 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:29)

rs_ID	r²[population]
rs11915333	1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs11918601	1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs11921624	1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs11923043	1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs17064511	1.00[EUR][1000 genomes]
rs3921997	1.00[EUR][1000 genomes]
rs58763528	1.00[EUR][1000 genomes]
rs60366187	1.00[EUR][1000 genomes]
rs61215023	1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs72877847	1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs72877848	1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs72877853	1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs72877855	1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs72877857	1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs72877859	1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs72877862	1.00[AMR][1000 genomes]
rs72877864	1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs72877876	1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs72877894	1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs72879804	1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs72879816	1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs72879862	1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs72879870	1.00[EUR][1000 genomes]
rs72879875	1.00[EUR][1000 genomes]
rs72879891	1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs72881709	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs72881734	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs7623666	1.00[EUR][1000 genomes]
rs7629722	1.00[EUR][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:8 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv876866	chr3:61054494-61310328	Weak transcription Enhancers Active TSS Flanking Active TSS ZNF genes & repeats Strong transcription Bivalent Enhancer Transcr. at gene 5' and 3' Genic enhancers	TF binding region CpG island Chromatin interactive region lncRNA	1 gene(s)	inside rSNPs	diseases
2	nsv876867	chr3:61054494-61474575	Weak transcription Enhancers Flanking Active TSS Active TSS Bivalent Enhancer ZNF genes & repeats Strong transcription Transcr. at gene 5' and 3' Genic enhancers	TF binding region CpG island Chromatin interactive region lncRNA	1 gene(s)	inside rSNPs	diseases
3	nsv432423	chr3:61100255-61606060	Enhancers Active TSS Weak transcription Flanking Active TSS Flanking Bivalent TSS/Enh Strong transcription Bivalent Enhancer Genic enhancers Bivalent/Poised TSS ZNF genes & repeats Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	9 gene(s)	inside rSNPs	diseases
4	nsv876868	chr3:61145050-61282503	Enhancers Flanking Active TSS Weak transcription Active TSS ZNF genes & repeats Transcr. at gene 5' and 3' Strong transcription Bivalent Enhancer Genic enhancers	TF binding region CpG island Chromatin interactive region lncRNA	1 gene(s)	inside rSNPs	diseases
5	nsv532626	chr3:61159646-61388418	Weak transcription Bivalent Enhancer Flanking Active TSS Enhancers Active TSS ZNF genes & repeats Genic enhancers Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	1 gene(s)	inside rSNPs	diseases
6	nsv1008399	chr3:61176965-61461349	Flanking Active TSS Enhancers Weak transcription ZNF genes & repeats Active TSS Transcr. at gene 5' and 3' Bivalent Enhancer Genic enhancers	TF binding region CpG island Chromatin interactive region lncRNA	1 gene(s)	inside rSNPs	diseases
7	nsv998982	chr3:61252469-61364001	Enhancers Weak transcription Flanking Active TSS ZNF genes & repeats Active TSS Bivalent Enhancer	Chromatin interactive region lncRNA	1 gene(s)	inside rSNPs	diseases
8	nsv979837	chr3:61265785-61282897	Enhancers Bivalent Enhancer Weak transcription	Chromatin interactive region	1 gene(s)	inside rSNPs	n/a

No data

Chromatin state (count:2 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr3:61261800-61269600	Weak transcription	Aorta	Aorta
2	chr3:61268200-61270400	Enhancers	Fetal Brain Male	brain

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