Variant report

rSNPs within LD-proxies of this variant (count:26)

rs_ID	r²[population]
rs1032554	0.96[ASN][1000 genomes]
rs12488855	0.96[ASN][1000 genomes]
rs12488882	0.96[ASN][1000 genomes]
rs12492495	0.96[ASN][1000 genomes]
rs12494700	0.93[ASN][1000 genomes]
rs13070192	0.89[ASN][1000 genomes]
rs13086095	0.96[AFR][1000 genomes];0.99[AMR][1000 genomes];0.93[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs13091778	0.96[ASN][1000 genomes]
rs13096806	0.93[ASN][1000 genomes]
rs13097372	0.89[ASN][1000 genomes]
rs13099485	0.93[ASN][1000 genomes]
rs1496616	0.99[AMR][1000 genomes];0.98[EUR][1000 genomes];0.93[ASN][1000 genomes]
rs17020153	0.96[ASN][1000 genomes]
rs2029920	0.98[AMR][1000 genomes];0.98[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs2088309	0.96[ASN][1000 genomes]
rs34617407	0.93[ASN][1000 genomes]
rs34641401	0.96[ASN][1000 genomes]
rs36046258	0.96[ASN][1000 genomes]
rs6548853	0.93[AFR][1000 genomes];0.99[AMR][1000 genomes];0.93[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs6781653	0.99[AMR][1000 genomes];0.93[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs6792836	0.96[ASN][1000 genomes]
rs71328419	0.89[ASN][1000 genomes]
rs7621875	0.93[ASN][1000 genomes]
rs9815966	0.96[ASN][1000 genomes]
rs9826203	0.94[AFR][1000 genomes];0.99[AMR][1000 genomes];0.99[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs9831888	1.00[CEU][hapmap];0.95[AFR][1000 genomes];0.99[AMR][1000 genomes];0.98[EUR][1000 genomes];1.00[ASN][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:2 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv1013820	chr3:82175705-82968181	Flanking Active TSS Enhancers Weak transcription Active TSS ZNF genes & repeats Bivalent/Poised TSS Bivalent Enhancer Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA	11 gene(s)	inside rSNPs	diseases
2	esv2830308	chr3:82741198-83269730	Enhancers Weak transcription Active TSS Flanking Active TSS Genic enhancers ZNF genes & repeats Bivalent Enhancer	TF binding region CpG island Chromatin interactive region 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	chr3:82838400-82840600	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
2	chr3:82839600-82840800	ZNF genes & repeats	iPS DF 19.11 Cell Line	embryonic stem cell

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