Variant report

Variant	rs8027984
Chromosome Location	chr15:54750464-54750465
allele	A/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 90 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:73)

rs_ID	r²[population]
rs11071082	0.92[AFR][1000 genomes];0.87[EUR][1000 genomes]
rs11071083	0.87[AFR][1000 genomes];0.87[EUR][1000 genomes]
rs11071084	0.91[AFR][1000 genomes];0.88[EUR][1000 genomes]
rs11071085	0.86[AFR][1000 genomes];0.82[EUR][1000 genomes]
rs11071086	0.86[AFR][1000 genomes];0.83[EUR][1000 genomes]
rs11635482	0.92[AFR][1000 genomes];0.88[EUR][1000 genomes]
rs11636568	0.93[AFR][1000 genomes];0.94[AMR][1000 genomes];0.97[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs11636573	0.92[AFR][1000 genomes];0.88[EUR][1000 genomes]
rs11854826	0.80[EUR][1000 genomes]
rs11858004	0.89[AFR][1000 genomes];0.94[AMR][1000 genomes];0.97[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs12148262	0.87[EUR][1000 genomes]
rs12437618	0.99[AFR][1000 genomes];0.90[EUR][1000 genomes]
rs12438368	0.99[AFR][1000 genomes];0.90[EUR][1000 genomes]
rs12439078	0.87[AFR][1000 genomes];0.84[EUR][1000 genomes]
rs12440914	0.86[EUR][1000 genomes]
rs12441633	0.99[AFR][1000 genomes];0.90[EUR][1000 genomes]
rs12442784	0.94[AMR][1000 genomes];0.97[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs12442847	0.94[AMR][1000 genomes];0.97[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs12592236	0.97[AFR][1000 genomes];0.90[EUR][1000 genomes]
rs12595197	0.81[AFR][1000 genomes];0.86[EUR][1000 genomes]
rs12595217	0.90[AFR][1000 genomes];0.87[EUR][1000 genomes]
rs12595229	0.82[AFR][1000 genomes];0.82[AMR][1000 genomes];0.81[EUR][1000 genomes];0.88[ASN][1000 genomes]
rs12900373	0.83[AFR][1000 genomes];0.84[EUR][1000 genomes]
rs12904002	0.93[AFR][1000 genomes];0.88[EUR][1000 genomes]
rs12907044	0.89[AFR][1000 genomes];0.87[EUR][1000 genomes]
rs12912159	0.87[EUR][1000 genomes]
rs12912401	0.87[EUR][1000 genomes]
rs12913695	0.84[EUR][1000 genomes]
rs12917122	0.82[AFR][1000 genomes];0.92[AMR][1000 genomes];0.99[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs1356859	0.90[AMR][1000 genomes];0.82[EUR][1000 genomes];0.94[ASN][1000 genomes]
rs1402112	0.90[AMR][1000 genomes];0.82[EUR][1000 genomes];0.94[ASN][1000 genomes]
rs1851004	0.91[AMR][1000 genomes];0.90[EUR][1000 genomes];0.93[ASN][1000 genomes]
rs2414308	0.97[AFR][1000 genomes];0.90[EUR][1000 genomes]
rs2414310	0.97[AMR][1000 genomes];0.98[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs2414314	0.83[EUR][1000 genomes]
rs2414321	0.87[AFR][1000 genomes];0.88[EUR][1000 genomes]
rs28390153	0.92[AFR][1000 genomes];0.88[EUR][1000 genomes]
rs28662893	0.92[AFR][1000 genomes];0.88[EUR][1000 genomes]
rs28675256	0.93[AFR][1000 genomes];0.92[AMR][1000 genomes];0.96[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs2899541	0.86[EUR][1000 genomes]
rs34298302	0.94[AMR][1000 genomes];0.98[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs4267255	0.89[AFR][1000 genomes];0.87[EUR][1000 genomes]
rs4457946	0.87[AFR][1000 genomes];0.88[EUR][1000 genomes]
rs4506836	0.92[AFR][1000 genomes];0.88[EUR][1000 genomes]
rs4641682	0.93[AFR][1000 genomes];0.94[AMR][1000 genomes];0.97[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs4774695	0.92[AFR][1000 genomes];0.88[EUR][1000 genomes]
rs4774696	0.92[AFR][1000 genomes];0.88[EUR][1000 genomes]
rs4774697	0.92[AFR][1000 genomes];0.88[EUR][1000 genomes]
rs4776231	0.96[AFR][1000 genomes];0.89[EUR][1000 genomes]
rs4776233	0.92[AFR][1000 genomes];0.88[EUR][1000 genomes]
rs5017619	0.89[AFR][1000 genomes];0.93[AMR][1000 genomes];0.94[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs5017620	0.89[AFR][1000 genomes];0.86[EUR][1000 genomes]
rs5017621	0.89[AFR][1000 genomes];0.86[EUR][1000 genomes]
rs5017622	0.89[AFR][1000 genomes];0.87[EUR][1000 genomes]
rs62022362	0.92[AFR][1000 genomes];0.87[EUR][1000 genomes]
rs62022363	0.92[AFR][1000 genomes];0.87[EUR][1000 genomes]
rs6493685	0.99[AFR][1000 genomes];0.90[EUR][1000 genomes]
rs71397588	0.80[AMR][1000 genomes]
rs7178299	0.93[AFR][1000 genomes];0.99[AMR][1000 genomes];0.99[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs7496778	0.87[EUR][1000 genomes]
rs8023474	0.93[AFR][1000 genomes];0.88[EUR][1000 genomes]
rs8023499	0.93[AFR][1000 genomes];0.94[AMR][1000 genomes];0.97[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs8024645	0.81[EUR][1000 genomes]
rs8024652	0.92[AFR][1000 genomes];0.88[EUR][1000 genomes]
rs8025195	0.88[AMR][1000 genomes];0.83[EUR][1000 genomes];0.95[ASN][1000 genomes]
rs8026344	0.87[EUR][1000 genomes]
rs8027041	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];0.99[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs8030561	0.97[AFR][1000 genomes];0.90[EUR][1000 genomes]
rs8033437	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];0.99[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs8038538	0.92[AFR][1000 genomes];0.88[EUR][1000 genomes]
rs8038792	0.92[AFR][1000 genomes];0.88[EUR][1000 genomes]
rs885203	0.90[AFR][1000 genomes];0.88[EUR][1000 genomes]
rs885204	0.92[AFR][1000 genomes];0.85[EUR][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:17 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv817539	chr15:54132584-55095235	Weak transcription Flanking Active TSS Enhancers Bivalent/Poised TSS Active TSS Flanking Bivalent TSS/Enh Genic enhancers ZNF genes & repeats Bivalent Enhancer Strong transcription	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	8 gene(s)	inside rSNPs	diseases
2	nsv904230	chr15:54685463-54779312	Enhancers Weak transcription ZNF genes & repeats	Chromatin interactive region lncRNA	1 gene(s)	inside rSNPs	diseases
3	nsv457150	chr15:54685463-54787358	Weak transcription Enhancers ZNF genes & repeats	Chromatin interactive region lncRNA	1 gene(s)	inside rSNPs	diseases
4	nsv569501	chr15:54685463-54787358	Weak transcription Enhancers ZNF genes & repeats	Chromatin interactive region lncRNA	1 gene(s)	inside rSNPs	diseases
5	nsv457151	chr15:54699197-54787358	ZNF genes & repeats Enhancers Weak transcription	Chromatin interactive region lncRNA	1 gene(s)	inside rSNPs	diseases
6	nsv569502	chr15:54699197-54787358	ZNF genes & repeats Weak transcription Enhancers	Chromatin interactive region lncRNA	1 gene(s)	inside rSNPs	diseases
7	nsv904231	chr15:54703195-54771880	ZNF genes & repeats Weak transcription Enhancers	Chromatin interactive region lncRNA	n/a	inside rSNPs	diseases
8	nsv904232	chr15:54703195-54787358	Enhancers ZNF genes & repeats Weak transcription	Chromatin interactive region lncRNA	1 gene(s)	inside rSNPs	diseases
9	nsv904233	chr15:54703195-54797177	Enhancers ZNF genes & repeats Weak transcription	TF binding region Chromatin interactive region lncRNA	2 gene(s)	inside rSNPs	diseases
10	nsv569503	chr15:54705902-54771880	Weak transcription Enhancers ZNF genes & repeats	Chromatin interactive region lncRNA	n/a	inside rSNPs	diseases
11	nsv457153	chr15:54705902-54795040	Enhancers ZNF genes & repeats Weak transcription	TF binding region Chromatin interactive region lncRNA	2 gene(s)	inside rSNPs	diseases
12	nsv569504	chr15:54705902-54795040	Enhancers Weak transcription ZNF genes & repeats	TF binding region Chromatin interactive region lncRNA	2 gene(s)	inside rSNPs	diseases
13	nsv904234	chr15:54710873-54779312	Weak transcription Enhancers ZNF genes & repeats	Chromatin interactive region	1 gene(s)	inside rSNPs	diseases
14	nsv904235	chr15:54710873-54795040	Weak transcription Enhancers ZNF genes & repeats	TF binding region Chromatin interactive region	2 gene(s)	inside rSNPs	diseases
15	nsv569505	chr15:54715550-54775229	Enhancers Weak transcription ZNF genes & repeats	Chromatin interactive region	n/a	inside rSNPs	diseases
16	nsv569506	chr15:54715550-54796592	Enhancers Weak transcription ZNF genes & repeats	TF binding region Chromatin interactive region	2 gene(s)	inside rSNPs	diseases
17	nsv569507	chr15:54730223-54787358	Weak transcription Enhancers ZNF genes & repeats	Chromatin interactive 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	chr15:54745600-54752200	Weak transcription	Aorta	Aorta

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