Variant report

rSNPs within LD-proxies of this variant (count:21)

rs_ID	r²[population]
rs12069481	0.94[CEU][hapmap]
rs12091733	0.89[EUR][1000 genomes]
rs1545007	0.94[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];1.00[YRI][hapmap]
rs16856811	0.86[EUR][1000 genomes]
rs16856830	0.94[CEU][hapmap];0.82[JPT][hapmap];0.94[EUR][1000 genomes]
rs1901357	0.92[EUR][1000 genomes]
rs2116517	0.98[AMR][1000 genomes];0.95[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs2568102	0.98[AFR][1000 genomes];0.93[AMR][1000 genomes];0.95[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs2599511	0.97[AFR][1000 genomes];0.95[AMR][1000 genomes];0.92[EUR][1000 genomes];0.95[ASN][1000 genomes]
rs2599512	0.91[AMR][1000 genomes];0.88[EUR][1000 genomes];0.95[ASN][1000 genomes]
rs2798412	0.95[AMR][1000 genomes];0.93[EUR][1000 genomes];0.95[ASN][1000 genomes]
rs2798415	0.99[AFR][1000 genomes];0.95[AMR][1000 genomes];0.95[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs2798418	0.98[AFR][1000 genomes];0.93[AMR][1000 genomes];0.95[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs3813991	0.87[EUR][1000 genomes]
rs55968043	0.94[EUR][1000 genomes]
rs60031791	0.94[EUR][1000 genomes]
rs6681161	0.94[CEU][hapmap]
rs6681310	0.94[CEU][hapmap];0.82[JPT][hapmap]
rs7524473	0.94[CEU][hapmap];0.82[JPT][hapmap]
rs919678	0.84[AFR][1000 genomes];0.99[ASN][1000 genomes]
rs919679	0.95[AMR][1000 genomes];0.95[EUR][1000 genomes];0.99[ASN][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:2 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv916491	chr1:166000783-166948513	Bivalent/Poised TSS Weak transcription Active TSS Enhancers Flanking Active TSS Genic enhancers Flanking Bivalent TSS/Enh Strong transcription Bivalent Enhancer Transcr. at gene 5' and 3' ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	38 gene(s)	inside rSNPs	diseases
2	esv3332610	chr1:166111288-166282689	Bivalent Enhancer Flanking Bivalent TSS/Enh Enhancers Weak transcription Flanking Active TSS Active TSS Bivalent/Poised TSS ZNF genes & repeats Transcr. at gene 5' and 3' Strong transcription	TF binding region CpG island Chromatin interactive region lncRNA miRNA	7 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:5 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr1:166251400-166253200	Enhancers	Skeletal Muscle Male	skeletal muscle
2	chr1:166251400-166253400	Enhancers	Liver	Liver
3	chr1:166251800-166253200	Enhancers	Skeletal Muscle Female	skeletal muscle
4	chr1:166252000-166252400	Enhancers	Right Atrium	heart
5	chr1:166252000-166252800	Enhancers	Left Ventricle	heart

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