Variant report

Variant	rs1814134
Chromosome Location	chr8:63013429-63013430
allele	G/T
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

No.	Distal block	Cell Line	Cell type	Cell Stage
1	chr8:63008246..63010935-chr8:63011772..63014314,2	K562	blood:

Extended variants
information (count: 52 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:49)

rs_ID	r²[population]
rs10107785	0.96[AFR][1000 genomes];0.98[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs1040195	0.97[AFR][1000 genomes];0.98[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs11990400	0.97[AMR][1000 genomes];1.00[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs1400506	0.95[AFR][1000 genomes];0.98[AMR][1000 genomes];0.99[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs1400512	0.87[AMR][1000 genomes];0.93[EUR][1000 genomes]
rs1516994	0.83[AMR][1000 genomes];0.91[EUR][1000 genomes]
rs1516995	0.87[AMR][1000 genomes];0.93[EUR][1000 genomes]
rs1546639	0.87[AMR][1000 genomes];0.95[EUR][1000 genomes]
rs1546640	0.86[AMR][1000 genomes];0.93[EUR][1000 genomes]
rs1607125	0.84[AMR][1000 genomes];0.92[EUR][1000 genomes]
rs1607132	0.90[AFR][1000 genomes];0.91[AMR][1000 genomes];0.99[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs2138642	0.97[AFR][1000 genomes];0.95[AMR][1000 genomes];0.99[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs2176346	0.99[AFR][1000 genomes];0.98[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs2203659	0.87[AMR][1000 genomes];0.93[EUR][1000 genomes]
rs2203660	0.88[EUR][1000 genomes]
rs2351083	0.84[AMR][1000 genomes];0.92[EUR][1000 genomes]
rs28634373	0.87[AMR][1000 genomes];0.95[EUR][1000 genomes]
rs28804830	0.84[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	0.87[AMR][1000 genomes];0.91[EUR][1000 genomes]
rs344264	0.84[AMR][1000 genomes];0.90[EUR][1000 genomes]
rs344265	0.84[AMR][1000 genomes];0.91[EUR][1000 genomes]
rs344266	0.84[AMR][1000 genomes];0.91[EUR][1000 genomes]
rs344267	0.84[AMR][1000 genomes];0.92[EUR][1000 genomes]
rs344271	0.90[EUR][1000 genomes]
rs35035266	0.87[AMR][1000 genomes];0.95[EUR][1000 genomes]
rs35999143	0.84[AMR][1000 genomes];0.89[EUR][1000 genomes]
rs55819473	0.87[AMR][1000 genomes];0.93[EUR][1000 genomes]
rs56098200	0.87[AMR][1000 genomes];0.95[EUR][1000 genomes]
rs57027979	0.87[AMR][1000 genomes];0.93[EUR][1000 genomes]
rs57232729	0.87[AMR][1000 genomes];0.93[EUR][1000 genomes]
rs59040850	0.84[AMR][1000 genomes];0.92[EUR][1000 genomes]
rs59691363	0.87[AMR][1000 genomes];0.95[EUR][1000 genomes]
rs61402923	0.87[AMR][1000 genomes];0.94[EUR][1000 genomes]
rs61475697	0.87[AMR][1000 genomes];0.95[EUR][1000 genomes]
rs62508546	0.84[AMR][1000 genomes];0.89[EUR][1000 genomes]
rs7814557	0.84[AMR][1000 genomes];0.92[EUR][1000 genomes]
rs7818829	0.87[AMR][1000 genomes];0.93[EUR][1000 genomes]
rs7832965	0.87[AMR][1000 genomes];0.93[EUR][1000 genomes]
rs9694964	0.84[AMR][1000 genomes];0.92[EUR][1000 genomes]
rs978254	0.97[AFR][1000 genomes];0.98[AMR][1000 genomes];1.00[EUR][1000 genomes];0.94[ASN][1000 genomes]
rs978255	0.97[AFR][1000 genomes];0.98[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs992841	0.84[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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