Variant report

No.	Distal block	Cell Line	Cell type	Cell Stage
1	chr2:31997008..31999119-chr2:32002900..32004751,2	K562	blood:

rSNPs within LD-proxies of this variant (count:27)

rs_ID	r²[population]
rs1090829	1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs11677520	1.00[AMR][1000 genomes]
rs11682335	1.00[CEU][hapmap];1.00[YRI][hapmap]
rs1397541	1.00[AMR][1000 genomes]
rs160793	1.00[CEU][hapmap];1.00[EUR][1000 genomes]
rs160794	0.82[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs160796	1.00[CEU][hapmap]
rs160810	1.00[AMR][1000 genomes];0.89[EUR][1000 genomes]
rs2093300	1.00[EUR][1000 genomes]
rs2116030	1.00[AMR][1000 genomes]
rs221195	1.00[CEU][hapmap];1.00[YRI][hapmap];1.00[AMR][1000 genomes];0.94[EUR][1000 genomes]
rs223618	1.00[EUR][1000 genomes]
rs223619	1.00[CEU][hapmap];1.00[YRI][hapmap];0.82[AFR][1000 genomes];1.00[EUR][1000 genomes]
rs223623	1.00[CEU][hapmap]
rs223624	1.00[CEU][hapmap];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs223654	1.00[EUR][1000 genomes]
rs223663	1.00[EUR][1000 genomes]
rs223664	1.00[CEU][hapmap]
rs413895	0.82[AFR][1000 genomes];1.00[AMR][1000 genomes];0.94[EUR][1000 genomes]
rs4141418	0.88[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs4952202	1.00[CEU][hapmap]
rs6543638	1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs6543639	1.00[EUR][1000 genomes]
rs6708897	0.89[EUR][1000 genomes]
rs7589874	1.00[CEU][hapmap];1.00[AMR][1000 genomes];0.88[EUR][1000 genomes]
rs806595	1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs806596	1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:5 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv532648	chr2:31591498-32312698	Weak transcription Enhancers Active TSS Flanking Active TSS Strong transcription ZNF genes & repeats Genic enhancers Flanking Bivalent TSS/Enh Bivalent/Poised TSS Bivalent Enhancer Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	39 gene(s)	inside rSNPs	diseases
2	esv3376782	chr2:31861607-32046180	Enhancers ZNF genes & repeats Weak transcription Active TSS Flanking Active TSS Strong transcription Bivalent Enhancer	TF binding region Chromatin interactive region lncRNA	7 gene(s)	inside rSNPs	diseases
3	nsv1003376	chr2:31889934-32022595	Enhancers Weak transcription Flanking Active TSS ZNF genes & repeats Active TSS	Chromatin interactive region lncRNA	3 gene(s)	inside rSNPs	diseases
4	nsv1015021	chr2:31972738-32030696	Enhancers Weak transcription	TF binding region Chromatin interactive region lncRNA	3 gene(s)	inside rSNPs	diseases
5	nsv963218	chr2:31997307-32013530	Enhancers Weak transcription	Chromatin interactive region lncRNA	1 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	chr2:32002200-32004600	Weak transcription	Right Atrium	heart

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