Variant report

Variant	rs7826370
Chromosome Location	chr8:3567268-3567269
allele	A/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 85 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:66)

rs_ID	r²[population]
rs10091302	0.95[CHB][hapmap];0.95[JPT][hapmap];0.90[AMR][1000 genomes];0.91[ASN][1000 genomes]
rs10092362	0.95[CHB][hapmap];0.95[JPT][hapmap];0.91[AMR][1000 genomes];0.97[ASN][1000 genomes]
rs10095969	0.85[CEU][hapmap];0.89[CHB][hapmap];0.94[JPT][hapmap]
rs10109819	0.91[AMR][1000 genomes];0.97[ASN][1000 genomes]
rs10112162	0.85[CHB][hapmap];0.80[JPT][hapmap];0.88[AMR][1000 genomes];0.90[ASN][1000 genomes]
rs11986814	0.88[CEU][hapmap];0.86[MEX][hapmap]
rs12541682	0.86[MEX][hapmap]
rs12681054	0.91[AFR][1000 genomes];0.98[AMR][1000 genomes];0.98[EUR][1000 genomes];0.94[ASN][1000 genomes]
rs12681058	0.91[AFR][1000 genomes];0.98[AMR][1000 genomes];0.97[EUR][1000 genomes];0.95[ASN][1000 genomes]
rs13253574	0.92[CEU][hapmap];0.86[CHB][hapmap];0.82[JPT][hapmap];0.86[MEX][hapmap];0.94[TSI][hapmap];0.81[EUR][1000 genomes];0.83[ASN][1000 genomes]
rs13254157	0.84[YRI][hapmap]
rs13256218	0.92[CEU][hapmap];0.91[CHB][hapmap];0.86[JPT][hapmap];0.89[TSI][hapmap]
rs13264352	0.80[CEU][hapmap];0.91[CHB][hapmap];0.86[JPT][hapmap];0.91[MEX][hapmap];0.94[TSI][hapmap];0.81[AMR][1000 genomes];0.81[EUR][1000 genomes];0.85[ASN][1000 genomes]
rs13269170	0.84[CEU][hapmap]
rs13273248	0.96[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];0.86[AFR][1000 genomes];0.96[AMR][1000 genomes];0.97[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs13273563	0.87[AFR][1000 genomes];0.96[AMR][1000 genomes];0.98[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs17067066	0.86[CHB][hapmap];0.82[JPT][hapmap];0.91[MEX][hapmap];0.83[AMR][1000 genomes];0.89[ASN][1000 genomes]
rs17326642	0.85[MEX][hapmap]
rs17326670	0.81[MEX][hapmap]
rs17326685	0.88[CEU][hapmap]
rs2291212	0.86[CHB][hapmap];0.82[JPT][hapmap];0.86[MEX][hapmap];0.85[AMR][1000 genomes];0.89[ASN][1000 genomes]
rs2291215	1.00[CEU][hapmap];0.91[CHB][hapmap];0.86[JPT][hapmap];0.86[YRI][hapmap]
rs2407122	0.91[CHB][hapmap];0.86[JPT][hapmap];0.83[ASN][1000 genomes]
rs34936899	0.87[AMR][1000 genomes];0.91[ASN][1000 genomes]
rs35962478	0.91[AMR][1000 genomes];0.94[ASN][1000 genomes]
rs4242518	0.88[CEU][hapmap];0.91[CHB][hapmap];0.86[JPT][hapmap];0.86[YRI][hapmap]
rs4304341	0.91[AMR][1000 genomes];0.95[ASN][1000 genomes]
rs4348525	0.90[CHB][hapmap];0.95[JPT][hapmap];0.92[AMR][1000 genomes];0.97[ASN][1000 genomes]
rs4355797	0.95[CHB][hapmap];0.95[JPT][hapmap];0.90[AMR][1000 genomes];0.95[ASN][1000 genomes]
rs4355798	0.90[CHB][hapmap];0.90[JPT][hapmap];0.90[AMR][1000 genomes];0.95[ASN][1000 genomes]
rs4398944	0.87[AMR][1000 genomes];0.91[ASN][1000 genomes]
rs4433172	0.90[CHB][hapmap];0.91[CHD][hapmap];0.95[JPT][hapmap];0.95[MEX][hapmap];0.92[AMR][1000 genomes];0.97[ASN][1000 genomes]
rs4443681	0.86[AMR][1000 genomes];0.95[ASN][1000 genomes]
rs4498582	0.88[AMR][1000 genomes];0.94[ASN][1000 genomes]
rs4518695	0.95[CHB][hapmap];0.95[JPT][hapmap];0.84[AMR][1000 genomes];0.95[ASN][1000 genomes]
rs4618717	0.90[AMR][1000 genomes];0.95[ASN][1000 genomes]
rs4875253	0.90[CHB][hapmap];0.89[JPT][hapmap];0.82[AMR][1000 genomes];0.84[ASN][1000 genomes]
rs4875254	1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];0.94[AMR][1000 genomes];0.98[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs4875772	0.86[CHB][hapmap];0.86[JPT][hapmap];0.85[ASN][1000 genomes]
rs4875773	0.85[CEU][hapmap];0.82[JPT][hapmap];0.83[LWK][hapmap];0.91[MEX][hapmap]
rs4875775	0.85[CEU][hapmap];0.82[JPT][hapmap];0.83[YRI][hapmap]
rs5003044	0.91[AMR][1000 genomes];0.97[ASN][1000 genomes]
rs5003045	0.91[AMR][1000 genomes];0.97[ASN][1000 genomes]
rs5003046	0.95[CHB][hapmap];0.95[JPT][hapmap];0.92[AMR][1000 genomes];0.97[ASN][1000 genomes]
rs5003047	0.95[CHB][hapmap];0.95[JPT][hapmap];0.91[AMR][1000 genomes];0.95[ASN][1000 genomes]
rs5003048	0.91[AMR][1000 genomes];0.95[ASN][1000 genomes]
rs5003049	0.91[AMR][1000 genomes];0.95[ASN][1000 genomes]
rs5022453	0.95[CHB][hapmap];0.95[JPT][hapmap];0.91[AMR][1000 genomes];0.95[ASN][1000 genomes]
rs62474754	0.85[AMR][1000 genomes];0.89[ASN][1000 genomes]
rs6984538	0.95[CHB][hapmap];0.90[JPT][hapmap]
rs6992262	0.85[CHB][hapmap];0.82[JPT][hapmap];0.83[ASN][1000 genomes]
rs7003458	0.91[CHB][hapmap];0.86[JPT][hapmap]
rs7005492	0.86[CHB][hapmap];0.82[JPT][hapmap]
rs7008391	0.95[CHB][hapmap];0.91[CHD][hapmap];0.90[JPT][hapmap];0.95[MEX][hapmap]
rs7012632	0.84[CHB][hapmap]
rs73185357	0.92[AMR][1000 genomes];0.95[ASN][1000 genomes]
rs73185372	0.92[AMR][1000 genomes];0.92[ASN][1000 genomes]
rs7462890	0.91[AMR][1000 genomes];0.94[ASN][1000 genomes]
rs7824746	0.88[CEU][hapmap]
rs7845193	0.96[AFR][1000 genomes];0.98[AMR][1000 genomes];0.99[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs876061	1.00[CHB][hapmap];1.00[JPT][hapmap]
rs878490	0.96[CEU][hapmap];0.86[CHB][hapmap];0.81[JPT][hapmap];0.83[YRI][hapmap]
rs900097	0.91[AMR][1000 genomes];0.95[ASN][1000 genomes]
rs900098	0.91[AMR][1000 genomes];0.94[ASN][1000 genomes]
rs900099	0.91[AMR][1000 genomes];0.94[ASN][1000 genomes]
rs9314503	0.95[CHB][hapmap];1.00[JPT][hapmap];0.82[AFR][1000 genomes];0.94[AMR][1000 genomes];0.97[ASN][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:19 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv1025209	chr8:3067655-3754882	Enhancers Flanking Active TSS Weak transcription Bivalent Enhancer Flanking Bivalent TSS/Enh Active TSS ZNF genes & repeats Strong transcription Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA	6 gene(s)	inside rSNPs	diseases
2	nsv1026998	chr8:3102679-3593264	Weak transcription Enhancers Strong transcription Flanking Active TSS Active TSS ZNF genes & repeats Bivalent Enhancer Flanking Bivalent TSS/Enh Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA	4 gene(s)	inside rSNPs	diseases
3	nsv1034076	chr8:3168033-3989947	Enhancers Weak transcription ZNF genes & repeats Flanking Active TSS Active TSS Bivalent Enhancer Flanking Bivalent TSS/Enh Strong transcription Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA	6 gene(s)	inside rSNPs	diseases
4	nsv539351	chr8:3168033-3989947	Active TSS Enhancers Weak transcription Flanking Active TSS ZNF genes & repeats Bivalent Enhancer Bivalent/Poised TSS Strong transcription Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA	6 gene(s)	inside rSNPs	diseases
5	nsv1017164	chr8:3174168-4026811	Enhancers Active TSS Weak transcription Flanking Active TSS ZNF genes & repeats Bivalent Enhancer Flanking Bivalent TSS/Enh Bivalent/Poised TSS Strong transcription	TF binding region CpG island Chromatin interactive region lncRNA	6 gene(s)	inside rSNPs	diseases
6	nsv539352	chr8:3174168-4026811	Enhancers Active TSS Weak transcription ZNF genes & repeats Strong transcription Flanking Active TSS Bivalent Enhancer Flanking Bivalent TSS/Enh Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA	6 gene(s)	inside rSNPs	diseases
7	nsv1018218	chr8:3180287-4089011	Active TSS Weak transcription Enhancers ZNF genes & repeats Bivalent Enhancer Flanking Active TSS Strong transcription Bivalent/Poised TSS Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA	6 gene(s)	inside rSNPs	diseases
8	nsv1028926	chr8:3318340-3667389	Enhancers Active TSS ZNF genes & repeats Weak transcription Flanking Active TSS Bivalent/Poised TSS Bivalent Enhancer	TF binding region CpG island Chromatin interactive region	5 gene(s)	inside rSNPs	diseases
9	nsv539353	chr8:3318340-3667389	Enhancers Active TSS ZNF genes & repeats Weak transcription Bivalent Enhancer Flanking Active TSS Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region	5 gene(s)	inside rSNPs	diseases
10	nsv831211	chr8:3504660-3660294	Enhancers Weak transcription Flanking Active TSS Active TSS ZNF genes & repeats Bivalent Enhancer Bivalent/Poised TSS	TF binding region Chromatin interactive region	5 gene(s)	inside rSNPs	diseases
11	nsv1017752	chr8:3530971-3754478	ZNF genes & repeats Enhancers Weak transcription Active TSS Flanking Active TSS Bivalent Enhancer Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region	4 gene(s)	inside rSNPs	diseases
12	nsv539355	chr8:3530971-3754478	Weak transcription Enhancers Bivalent Enhancer Flanking Active TSS Active TSS ZNF genes & repeats Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region	4 gene(s)	inside rSNPs	diseases
13	nsv1025204	chr8:3542586-3889592	Weak transcription Enhancers Active TSS Flanking Active TSS Bivalent Enhancer ZNF genes & repeats Bivalent/Poised TSS Strong transcription Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region	4 gene(s)	inside rSNPs	diseases
14	nsv539356	chr8:3542586-3889592	Weak transcription Enhancers Active TSS Flanking Active TSS Flanking Bivalent TSS/Enh ZNF genes & repeats Bivalent Enhancer Strong transcription Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region	4 gene(s)	inside rSNPs	diseases
15	nsv1022343	chr8:3553701-3578650	Enhancers Weak transcription Bivalent/Poised TSS	TF binding region	2 gene(s)	inside rSNPs	diseases
16	nsv949269	chr8:3556145-4246903	Enhancers Weak transcription Bivalent Enhancer Flanking Active TSS Active TSS ZNF genes & repeats Bivalent/Poised TSS Strong transcription Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region	5 gene(s)	inside rSNPs	diseases
17	nsv498034	chr8:3559289-3846288	Enhancers Active TSS Weak transcription Flanking Active TSS Bivalent Enhancer ZNF genes & repeats Bivalent/Poised TSS Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region	3 gene(s)	inside rSNPs	diseases
18	nsv889903	chr8:3560760-3575929	Enhancers Bivalent/Poised TSS Weak transcription	TF binding region	1 gene(s)	inside rSNPs	diseases
19	esv18414	chr8:3566776-3568330	Weak transcription Enhancers	TF binding region	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	chr8:3563200-3569400	Weak transcription	Cortex derived primary cultured neurospheres	brain

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