Variant report

Variant	rs59485845
Chromosome Location	chr10:96870316-96870317
allele	G/T
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 118 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:86)

rs_ID	r²[population]
rs1032097	1.00[EUR][1000 genomes]
rs1032098	1.00[EUR][1000 genomes]
rs11572073	1.00[EUR][1000 genomes]
rs11572081	1.00[EUR][1000 genomes]
rs11572089	1.00[EUR][1000 genomes]
rs11572132	1.00[EUR][1000 genomes]
rs11572145	1.00[EUR][1000 genomes]
rs11572148	1.00[EUR][1000 genomes]
rs11572176	1.00[EUR][1000 genomes]
rs11812764	1.00[EUR][1000 genomes]
rs11813834	1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs11814600	1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs11815378	1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs11816316	1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs11816732	1.00[EUR][1000 genomes]
rs11817176	1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs11817388	1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs11818420	1.00[AMR][1000 genomes]
rs11818486	1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs11819238	0.89[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs2094293	1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs2094294	0.89[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs2860950	1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs2860951	1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs45454292	1.00[EUR][1000 genomes]
rs45487391	1.00[EUR][1000 genomes]
rs45491002	1.00[EUR][1000 genomes]
rs45495404	1.00[EUR][1000 genomes]
rs45620737	1.00[EUR][1000 genomes]
rs55700247	1.00[EUR][1000 genomes]
rs55740007	1.00[EUR][1000 genomes]
rs55786415	1.00[EUR][1000 genomes]
rs55915838	1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs55937167	1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs56094588	1.00[EUR][1000 genomes]
rs56187632	0.90[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs56264187	1.00[EUR][1000 genomes]
rs56412102	1.00[EUR][1000 genomes]
rs56979418	0.88[AFR][1000 genomes];0.89[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs56999073	1.00[EUR][1000 genomes]
rs58894719	0.89[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs59277980	1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs59282006	1.00[EUR][1000 genomes]
rs59329992	0.89[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs59533405	1.00[EUR][1000 genomes]
rs60480656	1.00[EUR][1000 genomes]
rs60916665	1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs61478963	1.00[EUR][1000 genomes]
rs61634481	1.00[EUR][1000 genomes]
rs6583982	1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs6583986	1.00[EUR][1000 genomes]
rs7070484	1.00[EUR][1000 genomes]
rs7074994	1.00[EUR][1000 genomes]
rs7078505	1.00[EUR][1000 genomes]
rs7083576	1.00[EUR][1000 genomes]
rs7083837	1.00[EUR][1000 genomes]
rs7084045	1.00[EUR][1000 genomes]
rs7085646	1.00[EUR][1000 genomes]
rs7087494	1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs7088962	0.89[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs7090248	1.00[EUR][1000 genomes]
rs7090669	1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs7090961	1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs7091711	1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs7093626	0.89[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs7100479	1.00[EUR][1000 genomes]
rs74150750	1.00[EUR][1000 genomes]
rs74150764	1.00[EUR][1000 genomes]
rs74150766	1.00[EUR][1000 genomes]
rs74150767	1.00[EUR][1000 genomes]
rs74150768	1.00[EUR][1000 genomes]
rs74150772	1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs74150780	1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs74150781	1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs74150782	1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs74150785	1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs74150786	1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs74150790	0.89[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs74150792	1.00[EUR][1000 genomes]
rs74150793	1.00[EUR][1000 genomes]
rs74150795	1.00[EUR][1000 genomes]
rs7894207	1.00[EUR][1000 genomes]
rs7915255	1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs7918727	1.00[EUR][1000 genomes]
rs7918803	1.00[EUR][1000 genomes]
rs7919415	1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:32 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv497859	chr10:96058024-97027747	Strong transcription Weak transcription Active TSS Flanking Bivalent TSS/Enh Flanking Active TSS Enhancers ZNF genes & repeats Genic enhancers Bivalent/Poised TSS Transcr. at gene 5' and 3' Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	41 gene(s)	inside rSNPs	diseases
2	nsv529726	chr10:96632494-97106315	Strong transcription Enhancers Genic enhancers Flanking Bivalent TSS/Enh Bivalent Enhancer Weak transcription Flanking Active TSS Active TSS ZNF genes & repeats Bivalent/Poised TSS Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	15 gene(s)	inside rSNPs	diseases
3	nsv1043378	chr10:96855366-96876009	Enhancers Weak transcription Flanking Active TSS	n/a	n/a	inside rSNPs	diseases
4	esv21432	chr10:96856006-96996043	Weak transcription Strong transcription ZNF genes & repeats Enhancers Flanking Active TSS Genic enhancers Bivalent/Poised TSS Active TSS Bivalent Enhancer Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	5 gene(s)	inside rSNPs	diseases
5	nsv1040288	chr10:96857760-96876077	Weak transcription Flanking Active TSS Enhancers	n/a	n/a	inside rSNPs	diseases
6	nsv1040270	chr10:96857760-96882502	Enhancers ZNF genes & repeats Bivalent Enhancer Weak transcription Flanking Active TSS Active TSS	n/a	n/a	inside rSNPs	diseases
7	nsv7498	chr10:96857894-96881940	Enhancers Weak transcription Flanking Active TSS ZNF genes & repeats Active TSS	n/a	n/a	inside rSNPs	diseases
8	nsv1054199	chr10:96861570-96875702	Enhancers Flanking Active TSS Weak transcription	n/a	n/a	inside rSNPs	diseases
9	nsv1035517	chr10:96861570-96876009	Flanking Active TSS Enhancers Weak transcription	n/a	n/a	inside rSNPs	diseases
10	nsv551965	chr10:96864805-96872102	Enhancers Weak transcription	n/a	n/a	inside rSNPs	diseases
11	nsv551966	chr10:96864805-96874416	Enhancers Weak transcription	n/a	n/a	inside rSNPs	diseases
12	nsv437691	chr10:96864805-96876696	Enhancers Flanking Active TSS Weak transcription	n/a	n/a	inside rSNPs	diseases
13	esv15617	chr10:96864858-96874954	Weak transcription Enhancers	n/a	n/a	inside rSNPs	diseases
14	nsv1049012	chr10:96865081-96875947	Enhancers Flanking Active TSS Weak transcription	n/a	n/a	inside rSNPs	diseases
15	nsv1051425	chr10:96865081-96875963	Enhancers Flanking Active TSS Weak transcription	n/a	n/a	inside rSNPs	diseases
16	esv1792985	chr10:96865081-96876077	Enhancers Flanking Active TSS Weak transcription	n/a	n/a	inside rSNPs	diseases
17	esv1813761	chr10:96865081-96876077	Weak transcription Enhancers Flanking Active TSS	n/a	n/a	inside rSNPs	diseases
18	esv1828293	chr10:96865081-96876077	Weak transcription Flanking Active TSS Enhancers	n/a	n/a	inside rSNPs	diseases
19	esv1839838	chr10:96865081-96876077	Weak transcription Flanking Active TSS Enhancers	n/a	n/a	inside rSNPs	diseases
20	nsv1051877	chr10:96865081-96876077	Enhancers Flanking Active TSS Weak transcription	n/a	n/a	inside rSNPs	diseases
21	nsv1042421	chr10:96865081-96882502	Bivalent Enhancer Flanking Active TSS Weak transcription Enhancers ZNF genes & repeats Active TSS	n/a	n/a	inside rSNPs	diseases
22	nsv1046150	chr10:96865081-96885334	Weak transcription ZNF genes & repeats Enhancers Bivalent Enhancer Flanking Active TSS Active TSS	n/a	n/a	inside rSNPs	diseases
23	esv1837238	chr10:96865093-96876089	Enhancers Flanking Active TSS Weak transcription	n/a	n/a	inside rSNPs	diseases
24	nsv1041130	chr10:96865172-96882502	Bivalent Enhancer ZNF genes & repeats Weak transcription Enhancers Active TSS Flanking Active TSS	n/a	n/a	inside rSNPs	diseases
25	nsv1037640	chr10:96865196-96876077	Enhancers Flanking Active TSS Weak transcription	n/a	n/a	inside rSNPs	diseases
26	nsv436103	chr10:96866651-96875162	Enhancers Weak transcription	n/a	n/a	inside rSNPs	diseases
27	esv3316352	chr10:96867106-96875021	Enhancers Weak transcription	n/a	n/a	inside rSNPs	diseases
28	esv3316363	chr10:96867179-96874947	Enhancers Weak transcription	n/a	n/a	inside rSNPs	diseases
29	nsv498738	chr10:96867192-96874943	Weak transcription Enhancers	n/a	n/a	inside rSNPs	diseases
30	esv3316374	chr10:96867193-96874943	Enhancers Weak transcription	n/a	n/a	inside rSNPs	diseases
31	esv3318407	chr10:96869162-96873660	Enhancers Weak transcription	n/a	n/a	inside rSNPs	diseases
32	esv3318419	chr10:96869162-96873660	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	chr10:96869000-96871600	Enhancers	HepG2	liver

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