Variant report

rSNPs within LD-proxies of this variant (count:30)

rs_ID	r²[population]
rs10498980	0.85[ASN][1000 genomes]
rs10944604	0.94[EUR][1000 genomes]
rs16869979	0.83[ASN][1000 genomes]
rs16869986	0.85[ASN][1000 genomes]
rs16869990	0.85[ASN][1000 genomes]
rs16869995	0.91[ASN][1000 genomes]
rs16870004	0.82[AMR][1000 genomes];0.93[ASN][1000 genomes]
rs16870037	0.82[AMR][1000 genomes];0.93[ASN][1000 genomes]
rs1834730	0.83[ASN][1000 genomes]
rs2183002	0.82[AMR][1000 genomes];0.93[ASN][1000 genomes]
rs2261248	1.00[CHB][hapmap];1.00[JPT][hapmap]
rs2730835	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs2795079	0.84[AMR][1000 genomes];0.92[ASN][1000 genomes]
rs2860136	0.93[ASN][1000 genomes]
rs41339346	0.90[ASN][1000 genomes]
rs4706416	0.85[ASN][1000 genomes]
rs4706417	0.82[AMR][1000 genomes];0.89[ASN][1000 genomes]
rs4707745	0.88[ASN][1000 genomes]
rs56018944	0.85[ASN][1000 genomes]
rs58290198	0.85[ASN][1000 genomes]
rs6904770	0.82[ASN][1000 genomes]
rs6937226	0.83[ASN][1000 genomes]
rs72495305	0.82[ASN][1000 genomes]
rs72495306	0.82[ASN][1000 genomes]
rs73754313	0.85[ASN][1000 genomes]
rs783615	0.94[EUR][1000 genomes]
rs783849	0.94[AFR][1000 genomes];0.86[AMR][1000 genomes];0.99[ASN][1000 genomes]
rs783852	0.83[AFR][1000 genomes]
rs783863	0.84[AMR][1000 genomes];0.93[ASN][1000 genomes]
rs813656	0.81[AFR][1000 genomes];0.92[AMR][1000 genomes];0.96[EUR][1000 genomes];0.95[ASN][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	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
5	nsv886357	chr6:93274584-93348842	Enhancers Weak transcription Active TSS ZNF genes & repeats	lncRNA	n/a	inside rSNPs	diseases

No data

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

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr6:93276600-93277800	Weak transcription	Fetal Heart	heart

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