Variant report

rSNPs within LD-proxies of this variant (count:34)

rs_ID	r²[population]
rs10228341	0.93[AFR][1000 genomes];1.00[AMR][1000 genomes];0.89[EUR][1000 genomes];0.91[ASN][1000 genomes]
rs10235695	0.89[AMR][1000 genomes]
rs10247184	0.82[ASN][1000 genomes]
rs10252839	0.89[AMR][1000 genomes]
rs10253169	0.89[AMR][1000 genomes]
rs10266268	0.89[AMR][1000 genomes]
rs10268296	0.89[AMR][1000 genomes]
rs10268558	0.89[AMR][1000 genomes]
rs10277107	0.89[AMR][1000 genomes]
rs10281987	0.89[AMR][1000 genomes]
rs10441039	0.89[AFR][1000 genomes];1.00[AMR][1000 genomes];0.89[EUR][1000 genomes];0.91[ASN][1000 genomes]
rs10486312	0.89[AMR][1000 genomes]
rs12113191	1.00[AMR][1000 genomes];0.89[EUR][1000 genomes];0.91[ASN][1000 genomes]
rs12700004	0.89[EUR][1000 genomes]
rs12700005	0.89[EUR][1000 genomes]
rs12700006	0.89[AMR][1000 genomes]
rs12700009	0.89[AMR][1000 genomes]
rs13221164	0.89[AMR][1000 genomes]
rs13224833	0.89[AMR][1000 genomes]
rs13234557	0.89[EUR][1000 genomes]
rs13235810	0.89[AMR][1000 genomes]
rs13238305	0.89[EUR][1000 genomes]
rs13241140	0.89[AMR][1000 genomes]
rs13438582	0.89[AMR][1000 genomes]
rs17140193	0.89[AMR][1000 genomes]
rs17140198	0.89[AMR][1000 genomes]
rs34707237	0.88[AFR][1000 genomes];0.90[AMR][1000 genomes];1.00[EUR][1000 genomes];0.91[ASN][1000 genomes]
rs35024729	0.90[AFR][1000 genomes];0.90[AMR][1000 genomes];1.00[EUR][1000 genomes];0.91[ASN][1000 genomes]
rs59593404	0.94[ASN][1000 genomes]
rs59618106	0.91[ASN][1000 genomes]
rs73312680	0.81[ASN][1000 genomes]
rs7808375	0.89[AMR][1000 genomes]
rs7809412	0.89[AMR][1000 genomes]
rs7811828	0.89[AMR][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:5 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv498112	chr7:18677922-18991946	Weak transcription Enhancers Active TSS Flanking Active TSS Strong transcription Genic enhancers ZNF genes & repeats Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA	5 gene(s)	inside rSNPs	diseases
2	nsv887813	chr7:18720135-18995552	Enhancers Weak transcription Active TSS Flanking Active TSS Bivalent Enhancer ZNF genes & repeats Strong transcription Genic enhancers	TF binding region CpG island Chromatin interactive region lncRNA	4 gene(s)	inside rSNPs	diseases
3	nsv523497	chr7:18896011-18959381	Weak transcription Flanking Active TSS Genic enhancers Enhancers ZNF genes & repeats Active TSS	TF binding region CpG island lncRNA	1 gene(s)	inside rSNPs	diseases
4	esv2756248	chr7:18911960-18977760	Enhancers Weak transcription Flanking Active TSS Active TSS Genic enhancers ZNF genes & repeats	TF binding region CpG island lncRNA	1 gene(s)	inside rSNPs	diseases
5	nsv1030062	chr7:18915874-18943409	Weak transcription Enhancers Genic enhancers Flanking Active TSS Active TSS	TF binding region CpG island 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	chr7:18903000-18940000	Weak transcription	Aorta	Aorta
2	chr7:18906200-18929200	Weak transcription	Left Ventricle	heart

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