Variant report

rSNPs within LD-proxies of this variant (count:24)

rs_ID	r²[population]
rs10177883	0.85[EUR][1000 genomes]
rs13407248	0.91[ASN][1000 genomes]
rs1515294	0.93[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs16866934	0.82[EUR][1000 genomes]
rs16866936	0.83[EUR][1000 genomes]
rs16866942	0.93[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs16866944	0.87[AMR][1000 genomes];0.95[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs16866945	0.96[AMR][1000 genomes];0.96[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs17496658	0.87[EUR][1000 genomes];0.81[ASN][1000 genomes]
rs17499149	0.84[EUR][1000 genomes]
rs17499156	0.84[EUR][1000 genomes];0.81[ASN][1000 genomes]
rs1964081	0.89[EUR][1000 genomes];0.84[ASN][1000 genomes]
rs2840142	0.87[EUR][1000 genomes];0.81[ASN][1000 genomes]
rs56142641	0.85[EUR][1000 genomes]
rs58143036	0.84[EUR][1000 genomes]
rs59431424	0.88[EUR][1000 genomes];0.84[ASN][1000 genomes]
rs59642995	0.95[ASN][1000 genomes]
rs61200535	0.93[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs73973703	0.86[EUR][1000 genomes];0.81[ASN][1000 genomes]
rs746701	0.84[EUR][1000 genomes]
rs7582108	0.87[EUR][1000 genomes];0.86[ASN][1000 genomes]
rs7584651	0.98[ASN][1000 genomes]
rs7584968	0.98[ASN][1000 genomes]
rs881737	0.96[ASN][1000 genomes]

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

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv1002305	chr2:180568558-180812846	Enhancers Flanking Bivalent TSS/Enh Active TSS Weak transcription Bivalent/Poised TSS Bivalent Enhancer Strong transcription Flanking Active TSS ZNF genes & repeats Genic enhancers	TF binding region CpG island Chromatin interactive region lncRNA miRNA	6 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	chr2:180582400-180585600	Weak transcription	Right Atrium	heart

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