Variant report

rSNPs within LD-proxies of this variant (count:27)

rs_ID	r²[population]
rs13111601	0.82[AMR][1000 genomes]
rs13133420	0.82[AMR][1000 genomes];0.93[EUR][1000 genomes];0.94[ASN][1000 genomes]
rs13138590	1.00[AFR][1000 genomes];0.91[AMR][1000 genomes];0.93[EUR][1000 genomes];0.92[ASN][1000 genomes]
rs13143186	0.82[AMR][1000 genomes]
rs13143690	0.82[AMR][1000 genomes]
rs28457098	0.83[EUR][1000 genomes]
rs34267891	0.82[AMR][1000 genomes]
rs34384535	0.85[ASN][1000 genomes]
rs34455147	0.82[AMR][1000 genomes]
rs34533457	0.82[AMR][1000 genomes]
rs34746571	0.82[AMR][1000 genomes]
rs35117412	0.83[ASN][1000 genomes]
rs35649307	0.82[AMR][1000 genomes]
rs35856223	1.00[AFR][1000 genomes];0.91[AMR][1000 genomes];0.93[EUR][1000 genomes];0.87[ASN][1000 genomes]
rs36002786	1.00[AFR][1000 genomes];0.87[AMR][1000 genomes];0.90[EUR][1000 genomes];0.94[ASN][1000 genomes]
rs4505781	0.87[ASN][1000 genomes]
rs4621392	1.00[AFR][1000 genomes];0.91[AMR][1000 genomes];0.93[EUR][1000 genomes];0.94[ASN][1000 genomes]
rs61201051	0.82[AMR][1000 genomes]
rs61792873	0.85[ASN][1000 genomes]
rs61792935	1.00[AFR][1000 genomes];0.91[AMR][1000 genomes];0.93[EUR][1000 genomes];0.93[ASN][1000 genomes]
rs61792942	0.82[AMR][1000 genomes]
rs61792944	0.82[AMR][1000 genomes]
rs61792946	0.82[AMR][1000 genomes]
rs61792947	0.82[AMR][1000 genomes]
rs6819579	0.80[ASN][1000 genomes]
rs71598138	0.82[AMR][1000 genomes]
rs7696734	1.00[AFR][1000 genomes];0.91[AMR][1000 genomes];0.93[EUR][1000 genomes];0.94[ASN][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	nsv878810	chr4:30823157-30987395	Enhancers Weak transcription Flanking Active TSS Active TSS Genic enhancers Strong transcription ZNF genes & repeats	TF binding region CpG island Chromatin interactive region	3 gene(s)	inside rSNPs	diseases
2	nsv998450	chr4:30823631-31628179	Weak transcription Enhancers Genic enhancers Active TSS Flanking Active TSS ZNF genes & repeats Strong transcription Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	10 gene(s)	inside rSNPs	diseases
3	nsv963597	chr4:30980639-30981704	Weak transcription	n/a	n/a	inside rSNPs	n/a

No data

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

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr4:30928600-30997400	Weak transcription	Fetal Lung	lung
2	chr4:30964600-30992600	Weak transcription	Aorta	Aorta

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