Variant report

Variant	rs28792118
Chromosome Location	chr15:55237872-55237873
allele	A/C
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 99 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:87)

rs_ID	r²[population]
rs11071152	0.80[AMR][1000 genomes]
rs11071153	0.80[AMR][1000 genomes]
rs11071154	0.80[AMR][1000 genomes]
rs11071155	0.80[AMR][1000 genomes]
rs11071156	0.80[AMR][1000 genomes]
rs11071157	0.82[AFR][1000 genomes];0.91[AMR][1000 genomes]
rs11071158	0.82[AFR][1000 genomes];0.91[AMR][1000 genomes]
rs1915194	0.80[AMR][1000 genomes]
rs1915195	0.80[AMR][1000 genomes]
rs1915196	0.80[AMR][1000 genomes]
rs1915197	0.80[AMR][1000 genomes]
rs28413657	0.80[AMR][1000 genomes]
rs28419172	0.91[AMR][1000 genomes]
rs28433209	1.00[AMR][1000 genomes]
rs28433816	0.80[AMR][1000 genomes]
rs28436288	0.81[AFR][1000 genomes];0.91[AMR][1000 genomes]
rs28448273	0.91[AMR][1000 genomes]
rs28472405	0.81[AFR][1000 genomes];0.91[AMR][1000 genomes]
rs28482255	1.00[AMR][1000 genomes]
rs28485351	0.80[AMR][1000 genomes]
rs28491943	0.81[AFR][1000 genomes];0.91[AMR][1000 genomes]
rs28498890	0.81[AFR][1000 genomes];0.91[AMR][1000 genomes]
rs28508045	0.80[AMR][1000 genomes]
rs28514763	0.81[AFR][1000 genomes];0.91[AMR][1000 genomes]
rs28533686	0.80[AMR][1000 genomes]
rs28556619	0.81[AFR][1000 genomes];0.91[AMR][1000 genomes]
rs28576283	0.80[AMR][1000 genomes]
rs28581482	0.80[AMR][1000 genomes]
rs28581810	0.81[AFR][1000 genomes];0.91[AMR][1000 genomes]
rs28582762	0.91[AMR][1000 genomes]
rs28583904	0.80[AMR][1000 genomes]
rs28584748	0.80[AMR][1000 genomes]
rs28592965	0.80[AMR][1000 genomes]
rs28629359	0.81[AFR][1000 genomes];0.91[AMR][1000 genomes]
rs28642080	0.81[AFR][1000 genomes];0.91[AMR][1000 genomes]
rs28649002	0.80[AMR][1000 genomes]
rs28654296	0.80[AMR][1000 genomes]
rs28658200	0.83[AFR][1000 genomes];0.91[AMR][1000 genomes]
rs28676993	0.91[AMR][1000 genomes]
rs28694787	0.80[AMR][1000 genomes]
rs28715009	0.81[AFR][1000 genomes];0.91[AMR][1000 genomes]
rs28738738	0.91[AMR][1000 genomes]
rs28738833	0.80[AMR][1000 genomes]
rs28757879	0.81[AFR][1000 genomes];0.91[AMR][1000 genomes]
rs28764881	0.81[AFR][1000 genomes];0.91[AMR][1000 genomes]
rs28773263	1.00[AMR][1000 genomes]
rs28780794	0.87[AFR][1000 genomes];0.91[AMR][1000 genomes];1.00[ASN][1000 genomes]
rs28791772	1.00[AMR][1000 genomes];1.00[ASN][1000 genomes]
rs28795450	0.87[AFR][1000 genomes];0.91[AMR][1000 genomes]
rs28804781	0.95[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs28815830	0.83[AFR][1000 genomes];0.91[AMR][1000 genomes]
rs28823704	0.81[AFR][1000 genomes];0.91[AMR][1000 genomes]
rs28829938	0.95[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs28833523	0.92[AFR][1000 genomes];0.91[AMR][1000 genomes]
rs28833842	1.00[AMR][1000 genomes];1.00[ASN][1000 genomes]
rs28858199	0.80[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs28863785	0.86[AFR][1000 genomes];0.91[AMR][1000 genomes]
rs28869017	1.00[AMR][1000 genomes];1.00[ASN][1000 genomes]
rs28869178	0.91[AMR][1000 genomes]
rs28873169	0.90[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs28878200	0.83[AFR][1000 genomes];0.91[AMR][1000 genomes]
rs28881802	1.00[AMR][1000 genomes];1.00[ASN][1000 genomes]
rs28881888	0.90[AFR][1000 genomes];0.91[AMR][1000 genomes]
rs28886108	0.81[AFR][1000 genomes];0.91[AMR][1000 genomes]
rs28895618	0.88[AFR][1000 genomes];0.91[AMR][1000 genomes]
rs28896178	0.91[AMR][1000 genomes];1.00[ASN][1000 genomes]
rs56036017	0.80[AMR][1000 genomes]
rs6493729	0.80[AMR][1000 genomes]
rs6493731	0.80[AMR][1000 genomes]
rs6493732	0.80[AMR][1000 genomes]
rs7162099	0.83[AFR][1000 genomes];0.91[AMR][1000 genomes]
rs7162128	0.83[AFR][1000 genomes];0.91[AMR][1000 genomes]
rs7165315	0.80[AMR][1000 genomes]
rs7179591	1.00[AMR][1000 genomes]
rs74015033	1.00[AMR][1000 genomes]
rs74015034	0.83[AFR][1000 genomes];0.91[AMR][1000 genomes]
rs74015036	0.80[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs74015037	0.83[AFR][1000 genomes];0.91[AMR][1000 genomes]
rs7496492	0.81[AFR][1000 genomes];0.91[AMR][1000 genomes]
rs8024727	0.86[AFR][1000 genomes];0.91[AMR][1000 genomes]
rs8034234	0.80[AMR][1000 genomes]
rs8034854	0.91[AMR][1000 genomes]
rs8035888	0.91[AMR][1000 genomes]
rs8042097	0.80[AMR][1000 genomes]
rs8042111	0.80[AMR][1000 genomes]
rs8042496	0.80[AMR][1000 genomes]
rs9920978	0.91[AMR][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:12 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv1035785	chr15:54951691-55266222	Enhancers Flanking Active TSS Weak transcription Active TSS ZNF genes & repeats	Chromatin interactive region lncRNA	2 gene(s)	inside rSNPs	diseases
2	nsv542390	chr15:54951691-55266222	Enhancers Weak transcription Active TSS ZNF genes & repeats Flanking Active TSS	Chromatin interactive region lncRNA	2 gene(s)	inside rSNPs	diseases
3	nsv1043176	chr15:55010228-55563000	Genic enhancers Active TSS Weak transcription Enhancers Transcr. at gene 5' and 3' Strong transcription Flanking Active TSS ZNF genes & repeats Flanking Bivalent TSS/Enh Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	21 gene(s)	inside rSNPs	diseases
4	nsv1042741	chr15:55068022-55622497	Strong transcription Weak transcription Flanking Active TSS Enhancers Active TSS Genic enhancers ZNF genes & repeats Bivalent/Poised TSS Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	31 gene(s)	inside rSNPs	diseases
5	nsv1047424	chr15:55098585-55243518	Enhancers Active TSS Weak transcription ZNF genes & repeats Flanking Active TSS	Chromatin interactive region lncRNA	1 gene(s)	inside rSNPs	diseases
6	nsv833014	chr15:55099183-55249491	Enhancers ZNF genes & repeats Weak transcription Flanking Active TSS Active TSS	Chromatin interactive region lncRNA	1 gene(s)	inside rSNPs	diseases
7	nsv1039471	chr15:55137606-55552555	Enhancers Strong transcription Weak transcription Active TSS Flanking Active TSS Genic enhancers Bivalent/Poised TSS ZNF genes & repeats Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	20 gene(s)	inside rSNPs	diseases
8	nsv904239	chr15:55141265-55272996	Enhancers ZNF genes & repeats Weak transcription Flanking Active TSS Active TSS	Chromatin interactive region lncRNA	n/a	inside rSNPs	diseases
9	nsv569520	chr15:55170999-55327439	Enhancers Flanking Active TSS ZNF genes & repeats Weak transcription Active TSS	Chromatin interactive region lncRNA	n/a	inside rSNPs	diseases
10	nsv1541	chr15:55190471-55247202	Enhancers Weak transcription	Chromatin interactive region lncRNA	n/a	inside rSNPs	diseases
11	nsv111	chr15:55208707-55247202	Weak transcription Enhancers	Chromatin interactive region lncRNA	n/a	inside rSNPs	diseases
12	nsv9268	chr15:55233628-55243925	Enhancers Weak transcription	n/a	n/a	inside rSNPs	diseases

No data

Chromatin state (count:1 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr15:55225200-55252800	Weak transcription	Aorta	Aorta

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