Variant report

rSNPs within LD-proxies of this variant (count:27)

rs_ID	r²[population]
rs10137336	0.92[EUR][1000 genomes];0.89[ASN][1000 genomes]
rs10146014	0.89[ASN][1000 genomes]
rs10149682	0.89[ASN][1000 genomes]
rs10149704	0.96[ASN][1000 genomes]
rs10150517	0.91[ASN][1000 genomes]
rs12586637	0.87[ASN][1000 genomes]
rs12588002	0.91[ASN][1000 genomes]
rs1511318	0.86[AMR][1000 genomes];0.97[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs1705662	0.85[AFR][1000 genomes];0.95[AMR][1000 genomes];0.99[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs17119147	0.92[EUR][1000 genomes];0.89[ASN][1000 genomes]
rs17119189	0.85[ASN][1000 genomes]
rs17637116	0.89[ASN][1000 genomes]
rs17643817	0.89[ASN][1000 genomes]
rs17710375	0.91[ASN][1000 genomes]
rs17711443	0.89[ASN][1000 genomes]
rs17711598	0.89[ASN][1000 genomes]
rs28693875	0.93[ASN][1000 genomes]
rs55959064	0.85[ASN][1000 genomes]
rs57002888	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];0.99[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs59712100	0.88[AFR][1000 genomes];0.93[AMR][1000 genomes];0.96[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs7156850	0.87[ASN][1000 genomes]
rs72697171	0.96[AFR][1000 genomes];0.98[AMR][1000 genomes];0.99[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs72697173	0.98[AFR][1000 genomes];0.98[AMR][1000 genomes];0.99[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs72697185	0.87[ASN][1000 genomes]
rs8003162	0.82[AMR][1000 genomes];0.98[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs8003919	0.85[ASN][1000 genomes]
rs9323741	0.93[ASN][1000 genomes]

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	esv2758365	chr14:84136458-84293840	Enhancers Weak transcription Active TSS Flanking Active TSS ZNF genes & repeats	TF binding region CpG island Chromatin interactive region	2 gene(s)	inside rSNPs	diseases
2	esv2760003	chr14:84136458-84293840	Enhancers Weak transcription Active TSS Flanking Active TSS ZNF genes & repeats	TF binding region CpG island Chromatin interactive region	2 gene(s)	inside rSNPs	diseases
3	nsv832844	chr14:84136460-84293827	Enhancers Active TSS Weak transcription Flanking Active TSS ZNF genes & repeats	TF binding region CpG island Chromatin interactive region	2 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	chr14:84285000-84285200	Enhancers	Foreskin Melanocyte Primary Cells skin03	Skin

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