Variant report

Variant	rs1040195
Chromosome Location	chr8:63011498-63011499
allele	A/C
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 55 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:52)

rs_ID	r²[population]
rs10107785	0.98[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs11990400	0.82[AFR][1000 genomes];0.98[AMR][1000 genomes];1.00[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs1400506	0.97[AFR][1000 genomes];1.00[AMR][1000 genomes];0.99[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs1400512	0.89[AMR][1000 genomes];0.93[EUR][1000 genomes]
rs1516994	0.84[AMR][1000 genomes];0.91[EUR][1000 genomes]
rs1516995	0.89[AMR][1000 genomes];0.93[EUR][1000 genomes]
rs1546639	0.89[AMR][1000 genomes];0.95[EUR][1000 genomes]
rs1546640	0.81[AFR][1000 genomes];0.87[AMR][1000 genomes];0.93[EUR][1000 genomes]
rs1607125	0.86[AMR][1000 genomes];0.92[EUR][1000 genomes]
rs1607132	0.89[AFR][1000 genomes];0.92[AMR][1000 genomes];0.99[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs1814134	0.97[AFR][1000 genomes];0.98[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs2138642	0.96[AFR][1000 genomes];0.97[AMR][1000 genomes];0.99[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs2176346	0.98[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs2203659	0.89[AMR][1000 genomes];0.93[EUR][1000 genomes]
rs2203660	0.88[EUR][1000 genomes]
rs2351083	0.86[AMR][1000 genomes];0.92[EUR][1000 genomes]
rs28634373	0.89[AMR][1000 genomes];0.95[EUR][1000 genomes]
rs28804830	0.86[AMR][1000 genomes];0.92[EUR][1000 genomes]
rs344201	0.81[EUR][1000 genomes]
rs344205	0.89[EUR][1000 genomes]
rs344208	0.89[EUR][1000 genomes]
rs344243	0.89[EUR][1000 genomes]
rs344244	0.90[EUR][1000 genomes]
rs344249	0.90[EUR][1000 genomes]
rs344253	0.89[EUR][1000 genomes]
rs344263	0.89[AMR][1000 genomes];0.91[EUR][1000 genomes]
rs344264	0.86[AMR][1000 genomes];0.90[EUR][1000 genomes]
rs344265	0.86[AMR][1000 genomes];0.91[EUR][1000 genomes]
rs344266	0.86[AMR][1000 genomes];0.91[EUR][1000 genomes]
rs344267	0.86[AMR][1000 genomes];0.92[EUR][1000 genomes]
rs344271	0.90[EUR][1000 genomes]
rs35035266	0.89[AMR][1000 genomes];0.95[EUR][1000 genomes]
rs35999143	0.86[AMR][1000 genomes];0.89[EUR][1000 genomes]
rs55819473	0.89[AMR][1000 genomes];0.93[EUR][1000 genomes]
rs56098200	0.89[AMR][1000 genomes];0.95[EUR][1000 genomes]
rs57027979	0.89[AMR][1000 genomes];0.93[EUR][1000 genomes]
rs57232729	0.89[AMR][1000 genomes];0.93[EUR][1000 genomes]
rs59040850	0.86[AMR][1000 genomes];0.92[EUR][1000 genomes]
rs59691363	0.89[AMR][1000 genomes];0.95[EUR][1000 genomes]
rs61402923	0.89[AMR][1000 genomes];0.94[EUR][1000 genomes]
rs61475697	0.89[AMR][1000 genomes];0.95[EUR][1000 genomes]
rs62508546	0.86[AMR][1000 genomes];0.89[EUR][1000 genomes]
rs7814557	0.86[AMR][1000 genomes];0.92[EUR][1000 genomes]
rs7818020	0.83[CEU][hapmap]
rs7818029	0.82[CEU][hapmap]
rs7818829	0.89[AMR][1000 genomes];0.93[EUR][1000 genomes]
rs7832965	0.89[AMR][1000 genomes];0.93[EUR][1000 genomes]
rs7834120	0.86[CEU][hapmap]
rs9694964	0.86[AMR][1000 genomes];0.92[EUR][1000 genomes]
rs978254	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];0.94[ASN][1000 genomes]
rs978255	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs992841	0.86[AMR][1000 genomes];0.92[EUR][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	nsv890954	chr8:62919691-63023132	Enhancers Flanking Active TSS Active TSS Weak transcription Bivalent Enhancer Flanking Bivalent TSS/Enh ZNF genes & repeats Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA	1 gene(s)	inside rSNPs	diseases
2	nsv890955	chr8:62919691-63062581	Enhancers Flanking Active TSS Weak transcription Bivalent Enhancer Active TSS ZNF genes & repeats Bivalent/Poised TSS Flanking Bivalent TSS/Enh Strong transcription	TF binding region CpG island Chromatin interactive region lncRNA	2 gene(s)	inside rSNPs	diseases
3	nsv1032321	chr8:62954064-63026567	Enhancers Weak transcription ZNF genes & repeats	TF binding region Chromatin interactive region lncRNA	1 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	chr8:63009600-63013600	Weak transcription	Foreskin Melanocyte Primary Cells skin03	Skin

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