Variant report

rSNPs within LD-proxies of this variant (count:20)

rs_ID	r²[population]
rs11128091	0.82[EUR][1000 genomes]
rs12163576	0.86[EUR][1000 genomes]
rs13070250	0.96[AMR][1000 genomes];0.97[EUR][1000 genomes];0.95[ASN][1000 genomes]
rs1489996	0.83[EUR][1000 genomes]
rs1565385	0.97[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs17047969	0.88[AMR][1000 genomes];0.90[EUR][1000 genomes];0.90[ASN][1000 genomes]
rs1813868	0.82[EUR][1000 genomes]
rs2130438	0.89[AMR][1000 genomes];0.91[EUR][1000 genomes]
rs2171868	0.82[EUR][1000 genomes]
rs4855505	0.97[AMR][1000 genomes];1.00[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs56109105	0.87[EUR][1000 genomes]
rs56889723	0.84[EUR][1000 genomes]
rs57640416	0.82[EUR][1000 genomes]
rs58972171	0.82[EUR][1000 genomes]
rs59548135	0.82[EUR][1000 genomes]
rs62254074	0.84[ASN][1000 genomes]
rs72925108	0.87[EUR][1000 genomes]
rs7623995	0.82[EUR][1000 genomes]
rs870241	0.82[EUR][1000 genomes]
rs931433	0.80[EUR][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	nsv834722	chr3:68775036-68974120	Enhancers Bivalent Enhancer Weak transcription Bivalent/Poised TSS ZNF genes & repeats Active TSS Flanking Active TSS	TF binding region CpG island Chromatin interactive region	2 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:3 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr3:68799800-68808800	Weak transcription	Stomach Smooth Muscle	stomach
2	chr3:68801400-68807800	Weak transcription	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
3	chr3:68803600-68808000	Weak transcription	H9 Derived Neuron Cultured Cells	ES cell derived

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