Variant report

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

rs_ID	r²[population]
rs10455536	0.94[AMR][1000 genomes];1.00[EUR][1000 genomes];0.89[ASN][1000 genomes]
rs10755497	0.86[ASN][1000 genomes]
rs12191014	0.85[EUR][1000 genomes]
rs12213523	0.83[ASN][1000 genomes]
rs12216384	0.86[ASN][1000 genomes]
rs1328490	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs1427123	0.98[AFR][1000 genomes];0.97[AMR][1000 genomes];0.99[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs1590771	0.84[ASN][1000 genomes]
rs1590772	0.82[ASN][1000 genomes]
rs1927872	0.83[ASN][1000 genomes]
rs1927875	0.85[EUR][1000 genomes]
rs6899325	0.85[EUR][1000 genomes]
rs6899969	0.85[EUR][1000 genomes]
rs7753396	0.86[ASN][1000 genomes]
rs7758537	0.94[AMR][1000 genomes];0.99[EUR][1000 genomes];0.89[ASN][1000 genomes]
rs7762559	0.86[ASN][1000 genomes]
rs7771681	0.86[ASN][1000 genomes]
rs784066	0.94[AFR][1000 genomes];0.97[AMR][1000 genomes];0.99[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs809183	0.85[EUR][1000 genomes]
rs890559	0.98[AFR][1000 genomes];0.97[AMR][1000 genomes];0.98[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs9294533	0.86[ASN][1000 genomes]
rs9345243	0.89[ASN][1000 genomes]
rs9345246	0.86[ASN][1000 genomes]
rs9353921	0.81[AMR][1000 genomes];0.86[ASN][1000 genomes]
rs9353922	0.86[ASN][1000 genomes]
rs9362981	0.86[ASN][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:4 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	esv1845487	chr6:93099906-93306808	Enhancers Weak transcription Active TSS	TF binding region Chromatin interactive region lncRNA	3 gene(s)	inside rSNPs	diseases
2	nsv886355	chr6:93166766-93530757	Enhancers Weak transcription Flanking Active TSS ZNF genes & repeats Active TSS	TF binding region CpG island Chromatin interactive region lncRNA	4 gene(s)	inside rSNPs	diseases
3	nsv1018402	chr6:93173579-93855804	Enhancers Weak transcription ZNF genes & repeats Flanking Active TSS Active TSS Bivalent Enhancer Bivalent/Poised TSS Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA	12 gene(s)	inside rSNPs	diseases
4	nsv886356	chr6:93179624-93293303	Weak transcription Enhancers Active TSS	Chromatin interactive region	n/a	inside rSNPs	diseases

No data

Chromatin state (count:2 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr6:93250600-93254000	Weak transcription	HUVEC	blood vessel
2	chr6:93251200-93252400	Enhancers	Fetal Heart	heart

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