Variant report

Variant	rs4593565
Chromosome Location	chr8:4828706-4828707
allele	A/C
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 48 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:41)

rs_ID	r²[population]
rs10088688	1.00[CEU][hapmap];0.88[AMR][1000 genomes];0.91[EUR][1000 genomes]
rs10094549	0.90[CEU][hapmap]
rs10101412	0.95[CEU][hapmap];0.81[AMR][1000 genomes];0.90[EUR][1000 genomes]
rs10105362	0.89[CEU][hapmap]
rs1011587	1.00[CEU][hapmap];1.00[CHB][hapmap]
rs10503294	0.90[CEU][hapmap];0.81[EUR][1000 genomes]
rs10503296	0.90[CEU][hapmap];0.81[EUR][1000 genomes]
rs11136808	0.84[CEU][hapmap]
rs11778422	0.90[AMR][1000 genomes];0.92[EUR][1000 genomes]
rs12114470	0.90[CEU][hapmap]
rs12155630	0.90[CEU][hapmap];0.81[EUR][1000 genomes]
rs12674915	0.90[CEU][hapmap];0.81[EUR][1000 genomes]
rs13248218	0.90[CEU][hapmap]
rs13254311	0.93[CEU][hapmap]
rs13264559	1.00[CEU][hapmap];0.95[CHB][hapmap];1.00[YRI][hapmap]
rs13273154	0.90[CEU][hapmap]
rs2924719	0.90[CEU][hapmap]
rs2924720	1.00[CEU][hapmap];0.90[AMR][1000 genomes];0.90[EUR][1000 genomes]
rs2924721	0.90[AMR][1000 genomes];0.90[EUR][1000 genomes]
rs2924723	1.00[CEU][hapmap];0.90[AMR][1000 genomes];0.90[EUR][1000 genomes]
rs2924724	1.00[CEU][hapmap];0.88[AMR][1000 genomes];0.90[EUR][1000 genomes]
rs2977732	0.95[CEU][hapmap];0.85[AMR][1000 genomes]
rs2977733	0.85[CEU][hapmap]
rs4272399	0.88[AMR][1000 genomes];0.90[EUR][1000 genomes]
rs4278171	0.95[CEU][hapmap];0.95[CHB][hapmap];0.90[JPT][hapmap]
rs4295679	0.90[CEU][hapmap]
rs4329292	1.00[CEU][hapmap];0.96[CHB][hapmap]
rs4360313	0.90[CEU][hapmap]
rs4385481	0.90[CEU][hapmap]
rs4436145	0.87[AMR][1000 genomes];0.91[EUR][1000 genomes]
rs4477045	0.95[CEU][hapmap];0.88[AMR][1000 genomes];0.91[EUR][1000 genomes]
rs4495447	1.00[CEU][hapmap];0.90[AMR][1000 genomes];0.92[EUR][1000 genomes]
rs4517142	1.00[CEU][hapmap];0.85[AMR][1000 genomes];0.91[EUR][1000 genomes]
rs4517143	1.00[CEU][hapmap];0.85[AMR][1000 genomes];0.91[EUR][1000 genomes]
rs4521778	0.91[AMR][1000 genomes];0.83[EUR][1000 genomes]
rs4537322	0.86[CHB][hapmap]
rs4614018	1.00[CEU][hapmap];0.88[AMR][1000 genomes];0.91[EUR][1000 genomes]
rs4623447	0.90[CEU][hapmap];0.81[EUR][1000 genomes]
rs4875426	1.00[CEU][hapmap];0.85[AMR][1000 genomes];0.91[EUR][1000 genomes]
rs4875427	1.00[CEU][hapmap];0.92[AMR][1000 genomes];0.91[EUR][1000 genomes]
rs6558951	1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[YRI][hapmap]

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	nsv609876	chr8:4494811-5092970	Bivalent Enhancer Flanking Bivalent TSS/Enh Enhancers Bivalent/Poised TSS Weak transcription Flanking Active TSS Active TSS ZNF genes & repeats Strong transcription	TF binding region CpG island Chromatin interactive region lncRNA	5 gene(s)	inside rSNPs	diseases
2	nsv1029480	chr8:4497596-5081032	Enhancers Weak transcription Bivalent Enhancer Flanking Bivalent TSS/Enh Bivalent/Poised TSS Active TSS Flanking Active TSS ZNF genes & repeats Strong transcription	TF binding region CpG island Chromatin interactive region lncRNA	5 gene(s)	inside rSNPs	diseases
3	nsv498130	chr8:4532988-5176376	Active TSS Enhancers Flanking Bivalent TSS/Enh Bivalent Enhancer Flanking Active TSS ZNF genes & repeats Weak transcription Strong transcription Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA	5 gene(s)	inside rSNPs	diseases
4	nsv1031026	chr8:4771072-5054326	Bivalent Enhancer Flanking Bivalent TSS/Enh Weak transcription Bivalent/Poised TSS Enhancers Active TSS Flanking Active TSS ZNF genes & repeats Strong transcription	TF binding region CpG island Chromatin interactive region lncRNA	4 gene(s)	inside rSNPs	diseases
5	nsv1025322	chr8:4818393-4829588	Enhancers Weak transcription	Chromatin interactive region	n/a	inside rSNPs	diseases
6	nsv1028164	chr8:4818462-4829588	Enhancers Weak transcription	Chromatin interactive region	n/a	inside rSNPs	diseases
7	nsv1031402	chr8:4827087-4842934	Strong transcription Enhancers Weak transcription Active TSS	Chromatin interactive region	n/a	inside rSNPs	diseases

No data

Chromatin state (count:0 , 50 per page) page:

No data

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dbSNP/dbVar ID: rs12345 /nsv7879
a single nucleotide as 0-based coordinates: chr1:12345
chromosomal regions: chr1:12345-34567

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