Variant report

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

rs_ID	r²[population]
rs1410268	1.00[EUR][1000 genomes]
rs173240	1.00[EUR][1000 genomes]
rs189446	1.00[EUR][1000 genomes]
rs2769289	0.83[AFR][1000 genomes]
rs2770221	1.00[EUR][1000 genomes]
rs349123	0.88[AFR][1000 genomes];1.00[EUR][1000 genomes]
rs419815	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs57518020	1.00[EUR][1000 genomes]
rs7331838	1.00[EUR][1000 genomes]
rs74106504	1.00[EUR][1000 genomes]
rs7995650	1.00[ASW][hapmap]
rs884210	1.00[EUR][1000 genomes]
rs913396	1.00[EUR][1000 genomes]
rs9582148	1.00[EUR][1000 genomes]
rs9582149	1.00[EUR][1000 genomes]
rs9584614	0.88[AFR][1000 genomes];1.00[EUR][1000 genomes]
rs9584622	1.00[EUR][1000 genomes]
rs9584623	1.00[EUR][1000 genomes]
rs9584624	1.00[EUR][1000 genomes]
rs9584627	1.00[EUR][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:3 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv1139	chr13:98133793-98178130	Weak transcription Enhancers Bivalent Enhancer Flanking Active TSS	Chromatin interactive region	1 gene(s)	inside rSNPs	diseases
2	nsv1043113	chr13:98136208-98485012	Weak transcription Enhancers Active TSS Flanking Active TSS Bivalent Enhancer ZNF genes & repeats Genic enhancers Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA	2 gene(s)	inside rSNPs	diseases
3	nsv541884	chr13:98136208-98485012	Enhancers Weak transcription Flanking Active TSS ZNF genes & repeats Active TSS Bivalent Enhancer Bivalent/Poised TSS Genic enhancers	TF binding region CpG island Chromatin interactive region lncRNA	2 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	chr13:98175600-98179000	Weak transcription	HepG2	liver

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