Variant report

No.	Distal block	Cell Line	Cell type
1	chr4:110693557..110696333-chr4:110710067..110712118,2	K562	blood:
2	chr4:110684221..110686871-chr4:110694444..110697406,3	K562	blood:
3	chr4:110689596..110692531-chr4:110693989..110695768,2	K562	blood:

rSNPs within LD-proxies of this variant (count:34)

rs_ID	r²[population]
rs1000954	0.86[EUR][1000 genomes]
rs10016598	0.89[EUR][1000 genomes];0.85[ASN][1000 genomes]
rs10049804	0.88[EUR][1000 genomes];0.87[ASN][1000 genomes]
rs10857001	0.87[EUR][1000 genomes];0.87[ASN][1000 genomes]
rs11726234	0.86[EUR][1000 genomes]
rs11734208	1.00[ASN][1000 genomes]
rs12498247	0.88[EUR][1000 genomes]
rs12499926	0.85[EUR][1000 genomes]
rs12506605	0.88[EUR][1000 genomes]
rs12508074	0.86[EUR][1000 genomes]
rs12512308	0.91[EUR][1000 genomes]
rs13108145	0.99[ASN][1000 genomes]
rs13129180	1.00[ASN][1000 genomes]
rs28880991	0.86[EUR][1000 genomes]
rs4299581	0.92[AMR][1000 genomes];0.96[EUR][1000 genomes];0.87[ASN][1000 genomes]
rs4339213	0.90[AMR][1000 genomes];0.95[EUR][1000 genomes]
rs4371619	0.81[AMR][1000 genomes];0.86[EUR][1000 genomes]
rs4404543	1.00[ASN][1000 genomes]
rs4469075	0.90[ASN][1000 genomes]
rs4600912	0.81[AMR][1000 genomes];0.86[EUR][1000 genomes]
rs4698790	0.91[AMR][1000 genomes];0.96[EUR][1000 genomes];0.87[ASN][1000 genomes]
rs4698792	0.85[EUR][1000 genomes]
rs62324937	0.86[EUR][1000 genomes]
rs6815517	0.85[EUR][1000 genomes]
rs6841303	0.84[AMR][1000 genomes]
rs72674894	0.85[EUR][1000 genomes]
rs72674895	0.86[EUR][1000 genomes]
rs72674896	0.86[EUR][1000 genomes]
rs7439356	1.00[ASN][1000 genomes]
rs7440009	0.84[AMR][1000 genomes]
rs7442601	0.94[ASN][1000 genomes]
rs7659870	0.91[EUR][1000 genomes]
rs7671905	0.91[AMR][1000 genomes];0.93[EUR][1000 genomes]
rs9654197	0.89[EUR][1000 genomes];0.86[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	esv3349784	chr4:110348873-110723163	Enhancers Flanking Active TSS Weak transcription ZNF genes & repeats Active TSS Strong transcription Genic enhancers Flanking Bivalent TSS/Enh Bivalent Enhancer Transcr. at gene 5' and 3' Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	35 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	chr4:110691400-110695400	Weak transcription	Liver	Liver

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