Variant report

Variant	rs7829079
Chromosome Location	chr8:51648812-51648813
allele	A/C
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 95 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:88)

rs_ID	r²[population]
rs10087228	1.00[ASN][1000 genomes]
rs10087953	0.89[AFR][1000 genomes];0.87[AMR][1000 genomes];0.85[EUR][1000 genomes];0.95[ASN][1000 genomes]
rs10097209	0.93[AFR][1000 genomes];0.91[AMR][1000 genomes];0.90[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs10097404	0.93[AFR][1000 genomes];0.82[AMR][1000 genomes];1.00[ASN][1000 genomes]
rs10099033	0.98[ASN][1000 genomes]
rs10101076	0.88[EUR][1000 genomes];0.94[ASN][1000 genomes]
rs10110050	0.85[ASN][1000 genomes]
rs10111045	0.94[AFR][1000 genomes];0.87[ASN][1000 genomes]
rs10216649	0.98[ASN][1000 genomes]
rs10429378	0.85[ASN][1000 genomes]
rs10958023	0.85[ASN][1000 genomes]
rs10958026	0.85[ASN][1000 genomes]
rs10958061	1.00[ASN][1000 genomes]
rs10958065	0.94[AFR][1000 genomes];0.96[AMR][1000 genomes];0.95[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs10958066	0.84[AMR][1000 genomes];0.83[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs10958140	0.85[AFR][1000 genomes];0.81[ASN][1000 genomes]
rs11785968	0.94[ASN][1000 genomes]
rs11997970	0.85[ASN][1000 genomes]
rs12542948	0.83[AFR][1000 genomes];0.81[ASN][1000 genomes]
rs12681280	0.94[AFR][1000 genomes];0.86[AMR][1000 genomes];0.99[ASN][1000 genomes]
rs12681303	0.90[AFR][1000 genomes];0.99[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs13250468	0.87[ASN][1000 genomes]
rs13251712	0.81[ASN][1000 genomes]
rs13251980	0.93[ASN][1000 genomes]
rs13252863	0.88[EUR][1000 genomes]
rs13258680	0.83[AFR][1000 genomes];0.81[ASN][1000 genomes]
rs13261493	0.86[AFR][1000 genomes];0.83[ASN][1000 genomes]
rs13263172	0.89[ASN][1000 genomes]
rs13271305	0.89[ASN][1000 genomes]
rs13277400	0.83[AFR][1000 genomes];0.81[ASN][1000 genomes]
rs1396377	0.85[ASN][1000 genomes]
rs1472907	0.84[EUR][1000 genomes];0.85[ASN][1000 genomes]
rs1484129	0.85[AFR][1000 genomes]
rs1508621	0.96[AFR][1000 genomes];0.82[AMR][1000 genomes];1.00[ASN][1000 genomes]
rs1508622	0.93[AFR][1000 genomes];0.96[AMR][1000 genomes];0.94[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs1508623	0.81[ASN][1000 genomes]
rs1567311	0.85[AFR][1000 genomes];0.89[AMR][1000 genomes];0.93[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs16915417	0.87[AFR][1000 genomes];0.83[ASN][1000 genomes]
rs1911835	0.96[AFR][1000 genomes];0.83[AMR][1000 genomes];0.82[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs2170856	0.86[AFR][1000 genomes];0.83[ASN][1000 genomes]
rs2170857	0.87[AFR][1000 genomes];0.83[ASN][1000 genomes]
rs2202797	0.85[ASN][1000 genomes]
rs2392761	0.87[AMR][1000 genomes];0.88[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs28470779	0.98[ASN][1000 genomes]
rs28647321	0.82[AFR][1000 genomes];0.98[ASN][1000 genomes]
rs28683156	0.81[EUR][1000 genomes];0.89[ASN][1000 genomes]
rs28815525	0.96[AFR][1000 genomes];0.99[AMR][1000 genomes];0.97[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs34486025	0.93[AFR][1000 genomes];0.82[AMR][1000 genomes];1.00[ASN][1000 genomes]
rs34871864	0.85[ASN][1000 genomes]
rs35521388	1.00[ASN][1000 genomes]
rs3999808	0.94[AFR][1000 genomes];1.00[ASN][1000 genomes]
rs4242462	0.81[ASN][1000 genomes]
rs4382493	0.89[AFR][1000 genomes];0.83[ASN][1000 genomes]
rs4422788	0.91[AFR][1000 genomes];0.83[ASN][1000 genomes]
rs4873153	0.85[ASN][1000 genomes]
rs4873155	0.94[ASN][1000 genomes]
rs4873479	0.83[AFR][1000 genomes];0.81[ASN][1000 genomes]
rs6473292	0.93[ASN][1000 genomes]
rs6473319	1.00[ASN][1000 genomes]
rs66730072	1.00[ASN][1000 genomes]
rs67729017	0.89[ASN][1000 genomes]
rs6981207	0.93[AFR][1000 genomes];0.81[EUR][1000 genomes];0.83[ASN][1000 genomes]
rs6981429	0.93[AFR][1000 genomes];0.81[EUR][1000 genomes];0.83[ASN][1000 genomes]
rs6985321	0.93[AFR][1000 genomes];0.81[EUR][1000 genomes];0.83[ASN][1000 genomes]
rs6987633	0.85[ASN][1000 genomes]
rs6991518	0.91[ASN][1000 genomes]
rs6992341	0.98[ASN][1000 genomes]
rs6992551	1.00[ASN][1000 genomes]
rs6999211	0.85[ASN][1000 genomes]
rs7002119	0.91[ASN][1000 genomes]
rs7009895	0.97[ASN][1000 genomes]
rs7011647	0.96[AFR][1000 genomes];0.96[AMR][1000 genomes];0.94[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs7012338	0.93[ASN][1000 genomes]
rs7013183	0.87[AMR][1000 genomes];0.86[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs7013366	0.85[ASN][1000 genomes]
rs7015370	0.85[AFR][1000 genomes];0.83[ASN][1000 genomes]
rs7018197	1.00[ASN][1000 genomes]
rs7460470	0.93[AFR][1000 genomes];0.82[AMR][1000 genomes];1.00[ASN][1000 genomes]
rs7812344	1.00[ASN][1000 genomes]
rs7820724	0.86[AFR][1000 genomes];0.83[ASN][1000 genomes]
rs7822224	0.93[AFR][1000 genomes];0.83[AMR][1000 genomes];0.82[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs7833823	0.86[AFR][1000 genomes];0.83[ASN][1000 genomes]
rs7834256	0.93[AFR][1000 genomes];0.96[AMR][1000 genomes];0.94[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs7834585	1.00[ASN][1000 genomes]
rs7844393	0.83[ASN][1000 genomes]
rs7845831	1.00[ASN][1000 genomes]
rs906656	0.89[EUR][1000 genomes]
rs936722	0.86[AFR][1000 genomes];0.81[ASN][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:7 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv948436	chr8:51115028-51917504	Enhancers Weak transcription Flanking Active TSS ZNF genes & repeats Active TSS Bivalent Enhancer Strong transcription Genic enhancers Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA	6 gene(s)	inside rSNPs	diseases
2	nsv531502	chr8:51390997-51703556	Enhancers Flanking Active TSS ZNF genes & repeats Weak transcription Active TSS Strong transcription Genic enhancers	TF binding region CpG island Chromatin interactive region lncRNA	4 gene(s)	inside rSNPs	diseases
3	esv3514165	chr8:51416583-51923545	Enhancers Weak transcription ZNF genes & repeats Flanking Active TSS Active TSS Strong transcription	TF binding region CpG island Chromatin interactive region lncRNA	5 gene(s)	inside rSNPs	diseases
4	esv3514166	chr8:51416583-51923545	Enhancers ZNF genes & repeats Weak transcription Flanking Active TSS Active TSS Strong transcription	TF binding region CpG island Chromatin interactive region lncRNA	5 gene(s)	inside rSNPs	diseases
5	nsv1027452	chr8:51525439-51725489	Enhancers Weak transcription ZNF genes & repeats Active TSS Flanking Active TSS	TF binding region CpG island Chromatin interactive region lncRNA	2 gene(s)	inside rSNPs	diseases
6	nsv1019760	chr8:51628619-51862150	Enhancers Weak transcription ZNF genes & repeats Flanking Active TSS Active TSS	TF binding region Chromatin interactive region lncRNA	2 gene(s)	inside rSNPs	diseases
7	nsv1029698	chr8:51628619-51863635	Weak transcription Enhancers ZNF genes & repeats Active TSS Flanking Active TSS	TF binding region Chromatin interactive region lncRNA	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	chr8:51648800-51649200	ZNF genes & repeats	Ganglion Eminence derived primary cultured neurospheres	brain

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