Variant report

rSNPs within LD-proxies of this variant (count:23)

rs_ID	r²[population]
rs11733661	0.85[YRI][hapmap]
rs12499967	0.96[AFR][1000 genomes];0.92[EUR][1000 genomes]
rs1390258	1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap]
rs1390260	0.80[LWK][hapmap]
rs1390262	1.00[CEU][hapmap]
rs1390264	1.00[CEU][hapmap];0.92[LWK][hapmap];0.98[MKK][hapmap];0.90[TSI][hapmap];0.81[YRI][hapmap];0.84[AFR][1000 genomes];0.92[EUR][1000 genomes]
rs1390266	1.00[CEU][hapmap];0.85[TSI][hapmap]
rs1495519	0.84[AFR][1000 genomes];0.92[EUR][1000 genomes]
rs1495520	1.00[CEU][hapmap];0.87[EUR][1000 genomes]
rs1826738	1.00[CEU][hapmap]
rs1845694	1.00[CEU][hapmap]
rs1948519	1.00[CEU][hapmap]
rs2322941	1.00[CEU][hapmap];0.90[TSI][hapmap]
rs2322958	1.00[CEU][hapmap];0.92[LWK][hapmap];0.98[MKK][hapmap];0.90[TSI][hapmap];0.81[YRI][hapmap];0.84[AFR][1000 genomes];0.92[EUR][1000 genomes]
rs2322959	1.00[CEU][hapmap];0.81[YRI][hapmap];0.84[AFR][1000 genomes];0.92[EUR][1000 genomes]
rs4618301	1.00[CEU][hapmap];1.00[CHB][hapmap];0.88[JPT][hapmap];0.92[YRI][hapmap]
rs4696976	1.00[CEU][hapmap];0.81[YRI][hapmap];0.83[AFR][1000 genomes];0.92[EUR][1000 genomes]
rs6854379	0.96[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs7655472	1.00[CEU][hapmap];0.83[AFR][1000 genomes];0.92[EUR][1000 genomes]
rs7657161	0.83[AFR][1000 genomes];0.92[EUR][1000 genomes]
rs7660556	1.00[CEU][hapmap]
rs7675173	1.00[CEU][hapmap];0.96[LWK][hapmap];0.96[MKK][hapmap];0.90[TSI][hapmap];0.81[YRI][hapmap];0.83[AFR][1000 genomes];0.92[EUR][1000 genomes]
rs9996172	1.00[CEU][hapmap]

Variant overlapped rSNPs/rCNVs (count:3 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv1013365	chr4:20834054-21609078	Bivalent/Poised TSS Flanking Active TSS Active TSS Weak transcription Enhancers Bivalent Enhancer Flanking Bivalent TSS/Enh Strong transcription ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA	4 gene(s)	inside rSNPs	diseases
2	nsv1014062	chr4:21270358-21479027	Bivalent Enhancer Flanking Bivalent TSS/Enh Flanking Active TSS Enhancers Weak transcription Active TSS Bivalent/Poised TSS ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA	2 gene(s)	inside rSNPs	diseases
3	nsv1005453	chr4:21295066-21454143	Enhancers Weak transcription Active TSS Bivalent/Poised TSS Bivalent Enhancer Flanking Active TSS Flanking Bivalent TSS/Enh ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA	2 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:0 , 50 per page) page:

No data

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