Variant report

rSNPs within LD-proxies of this variant (count:21)

rs_ID	r²[population]
rs11914686	1.00[ASN][1000 genomes]
rs11915075	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs13068053	1.00[ASN][1000 genomes]
rs13324837	1.00[ASN][1000 genomes]
rs1454265	1.00[ASN][1000 genomes]
rs28729280	1.00[ASN][1000 genomes]
rs35507461	1.00[ASN][1000 genomes]
rs35868610	1.00[ASN][1000 genomes]
rs58620671	1.00[ASN][1000 genomes]
rs59020662	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs6768918	1.00[ASN][1000 genomes]
rs6790295	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs73115805	1.00[ASN][1000 genomes]
rs73118693	1.00[ASN][1000 genomes]
rs73126649	1.00[ASN][1000 genomes]
rs73138243	1.00[ASN][1000 genomes]
rs7645586	1.00[ASN][1000 genomes]
rs9813850	1.00[ASN][1000 genomes]
rs9853565	1.00[ASN][1000 genomes]
rs9863575	1.00[ASN][1000 genomes]
rs9864451	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	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

No data

Chromatin state (count:4 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr3:82511000-82512000	Weak transcription	HUES64 Cell Line	embryonic stem cell
2	chr3:82511000-82512000	Weak transcription	Liver	Liver
3	chr3:82511000-82512000	Weak transcription	Dnd41	blood
4	chr3:82511400-82513400	Enhancers	HepG2	liver

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