Variant report

rSNPs within LD-proxies of this variant (count:25)

rs_ID	r²[population]
rs1012085	0.94[AFR][1000 genomes]
rs1146883	0.93[ASN][1000 genomes]
rs1146888	0.89[ASN][1000 genomes]
rs1146890	0.85[ASN][1000 genomes]
rs1505141	0.94[ASN][1000 genomes]
rs1700826	0.90[ASN][1000 genomes]
rs17066099	0.86[ASN][1000 genomes]
rs17685818	0.96[AFR][1000 genomes]
rs1847629	0.96[AFR][1000 genomes];1.00[AMR][1000 genomes];0.99[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs1929731	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];0.99[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs2657128	0.91[ASN][1000 genomes]
rs2777732	0.92[ASN][1000 genomes]
rs4142608	0.82[AMR][1000 genomes];0.89[ASN][1000 genomes]
rs4142610	0.82[AMR][1000 genomes];0.90[ASN][1000 genomes]
rs4646990	0.97[AFR][1000 genomes]
rs61963409	0.80[EUR][1000 genomes];0.90[ASN][1000 genomes]
rs7316936	0.97[AFR][1000 genomes]
rs7317053	0.97[AFR][1000 genomes]
rs7318308	0.97[AFR][1000 genomes]
rs7318915	0.97[AFR][1000 genomes]
rs8001163	0.87[AMR][1000 genomes];0.92[EUR][1000 genomes];0.90[ASN][1000 genomes]
rs9318421	0.84[ASN][1000 genomes]
rs9530536	0.86[ASN][1000 genomes]
rs9544242	0.91[AFR][1000 genomes]
rs9544243	0.97[AFR][1000 genomes];1.00[AMR][1000 genomes];0.99[EUR][1000 genomes];1.00[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	nsv1044736	chr13:76728655-77066435	Enhancers Flanking Active TSS Weak transcription Bivalent Enhancer ZNF genes & repeats Active TSS	Chromatin interactive region	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	chr13:76882000-76885600	Weak transcription	IMR90 fetal lung fibroblasts Cell Line	lung
2	chr13:76883200-76891200	Weak transcription	Fetal Heart	heart

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