Variant report

Variant	rs10786186
Chromosome Location	chr10:96855958-96855959
allele	A/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 157 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:146)

rs_ID	r²[population]
rs10128123	0.93[ASN][1000 genomes]
rs10218877	0.91[AMR][1000 genomes];0.93[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs10509682	0.97[AMR][1000 genomes];0.98[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs10509683	0.93[ASN][1000 genomes]
rs10786187	0.93[ASN][1000 genomes]
rs10786188	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];0.97[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs10786189	0.93[ASN][1000 genomes]
rs10786190	0.93[ASN][1000 genomes]
rs10882542	0.96[AFR][1000 genomes];0.98[AMR][1000 genomes];0.99[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs10882543	0.93[ASN][1000 genomes]
rs10882546	0.93[ASN][1000 genomes]
rs10882551	0.97[AMR][1000 genomes];0.98[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs10882562	0.94[AMR][1000 genomes];0.97[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs10882564	0.92[AMR][1000 genomes];0.91[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs10882565	0.92[AMR][1000 genomes];0.91[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs10882566	0.92[AMR][1000 genomes];0.94[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs10882568	0.93[ASN][1000 genomes]
rs10882569	0.86[ASN][1000 genomes]
rs11188189	0.93[ASN][1000 genomes]
rs11188190	0.93[ASN][1000 genomes]
rs11188192	0.93[ASN][1000 genomes]
rs11188196	0.93[ASN][1000 genomes]
rs11188197	0.93[ASN][1000 genomes]
rs11188200	0.93[ASN][1000 genomes]
rs11188214	0.83[AMR][1000 genomes];0.95[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs11188219	0.97[AMR][1000 genomes];0.97[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs11188223	0.95[AMR][1000 genomes];0.95[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs11188225	0.95[AMR][1000 genomes];0.95[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs11188227	0.93[ASN][1000 genomes]
rs11188228	0.93[ASN][1000 genomes]
rs11188229	0.93[ASN][1000 genomes]
rs11188230	0.85[ASN][1000 genomes]
rs11599884	0.93[ASN][1000 genomes]
rs12245722	0.93[ASN][1000 genomes]
rs12261370	0.93[ASN][1000 genomes]
rs12262878	0.93[ASN][1000 genomes]
rs12266386	0.92[AMR][1000 genomes];0.91[EUR][1000 genomes];0.89[ASN][1000 genomes]
rs12354433	0.95[AMR][1000 genomes];0.95[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs12769577	0.86[ASN][1000 genomes]
rs12769820	0.93[ASN][1000 genomes]
rs12782731	0.93[ASN][1000 genomes]
rs1575930	0.93[ASN][1000 genomes]
rs16872	0.93[ASN][1000 genomes]
rs17451604	0.95[AMR][1000 genomes];0.95[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs17524438	0.93[ASN][1000 genomes]
rs2449809	0.93[ASN][1000 genomes]
rs2449810	0.93[ASN][1000 genomes]
rs2478477	0.90[ASN][1000 genomes]
rs2478478	0.93[ASN][1000 genomes]
rs2478479	0.93[ASN][1000 genomes]
rs2478480	0.86[ASN][1000 genomes]
rs2901829	0.93[ASN][1000 genomes]
rs34999658	0.97[AMR][1000 genomes];0.99[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs35306243	0.97[AMR][1000 genomes];0.99[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs35999600	0.93[ASN][1000 genomes]
rs4119640	0.81[ASN][1000 genomes]
rs4532969	0.93[ASN][1000 genomes]
rs489807	0.86[ASN][1000 genomes]
rs509736	0.86[ASN][1000 genomes]
rs513661	0.87[ASN][1000 genomes]
rs519833	0.86[ASN][1000 genomes]
rs585381	0.93[ASN][1000 genomes]
rs589801	0.86[ASN][1000 genomes]
rs591157	0.93[ASN][1000 genomes]
rs591171	0.86[ASN][1000 genomes]
rs593207	0.86[ASN][1000 genomes]
rs594402	0.93[ASN][1000 genomes]
rs594448	0.86[ASN][1000 genomes]
rs595420	0.86[ASN][1000 genomes]
rs595478	0.86[ASN][1000 genomes]
rs600929	0.86[ASN][1000 genomes]
rs602941	0.86[ASN][1000 genomes]
rs604022	0.93[ASN][1000 genomes]
rs604373	0.93[ASN][1000 genomes]
rs610046	0.93[ASN][1000 genomes]
rs610579	0.89[ASN][1000 genomes]
rs610837	0.86[ASN][1000 genomes]
rs611343	0.86[ASN][1000 genomes]
rs611371	0.86[ASN][1000 genomes]
rs611416	0.93[ASN][1000 genomes]
rs612490	0.86[ASN][1000 genomes]
rs613340	0.93[ASN][1000 genomes]
rs614682	0.93[ASN][1000 genomes]
rs620196	0.93[ASN][1000 genomes]
rs621299	0.86[ASN][1000 genomes]
rs626415	0.93[ASN][1000 genomes]
rs627173	0.86[ASN][1000 genomes]
rs627719	0.86[ASN][1000 genomes]
rs628102	0.86[ASN][1000 genomes]
rs631107	0.80[ASN][1000 genomes]
rs632113	0.93[ASN][1000 genomes]
rs632361	0.86[ASN][1000 genomes]
rs632979	0.82[ASN][1000 genomes]
rs633345	0.86[ASN][1000 genomes]
rs634269	0.93[ASN][1000 genomes]
rs637465	0.86[ASN][1000 genomes]
rs637724	0.93[ASN][1000 genomes]
rs637939	0.86[ASN][1000 genomes]
rs638895	0.93[ASN][1000 genomes]
rs641198	0.93[ASN][1000 genomes]
rs644437	0.93[ASN][1000 genomes]
rs646845	0.93[ASN][1000 genomes]
rs648638	0.93[ASN][1000 genomes]
rs648695	0.86[ASN][1000 genomes]
rs649770	0.83[ASN][1000 genomes]
rs6583980	0.93[ASN][1000 genomes]
rs659949	0.86[ASN][1000 genomes]
rs660026	0.86[ASN][1000 genomes]
rs663473	0.93[ASN][1000 genomes]
rs664093	0.86[ASN][1000 genomes]
rs666679	0.93[ASN][1000 genomes]
rs666786	0.93[ASN][1000 genomes]
rs667499	0.82[ASN][1000 genomes]
rs669360	0.86[ASN][1000 genomes]
rs672428	0.93[ASN][1000 genomes]
rs672860	0.93[ASN][1000 genomes]
rs675332	0.93[ASN][1000 genomes]
rs678165	0.93[ASN][1000 genomes]
rs679025	0.93[ASN][1000 genomes]
rs680918	0.93[ASN][1000 genomes]
rs682477	0.93[ASN][1000 genomes]
rs685607	0.86[ASN][1000 genomes]
rs688706	0.86[ASN][1000 genomes]
rs689207	0.86[ASN][1000 genomes]
rs701886	0.86[ASN][1000 genomes]
rs7079861	0.93[ASN][1000 genomes]
rs7082502	0.93[ASN][1000 genomes]
rs7087492	0.93[ASN][1000 genomes]
rs7087618	0.93[ASN][1000 genomes]
rs7089303	0.90[ASN][1000 genomes]
rs7094658	0.93[ASN][1000 genomes]
rs752415	0.93[ASN][1000 genomes]
rs752416	0.93[ASN][1000 genomes]
rs752417	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs7907627	0.93[ASN][1000 genomes]
rs7907827	0.93[ASN][1000 genomes]
rs7921561	0.93[ASN][1000 genomes]
rs815250	0.86[ASN][1000 genomes]
rs815265	0.93[ASN][1000 genomes]
rs815266	0.93[ASN][1000 genomes]
rs815267	0.82[ASN][1000 genomes]
rs815268	0.93[ASN][1000 genomes]
rs815269	0.93[ASN][1000 genomes]
rs815270	0.93[ASN][1000 genomes]
rs943313	0.93[ASN][1000 genomes]
rs943315	0.93[ASN][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:11 , 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	nsv467436	chr10:96805371-96862286	Genic enhancers Weak transcription Enhancers Active TSS Strong transcription Flanking Active TSS ZNF genes & repeats Transcr. at gene 5' and 3'	TF binding region CpG island	1 gene(s)	inside rSNPs	diseases
4	nsv551964	chr10:96805371-96862286	ZNF genes & repeats Strong transcription Genic enhancers Active TSS Enhancers Weak transcription Flanking Active TSS Transcr. at gene 5' and 3'	TF binding region CpG island	1 gene(s)	inside rSNPs	diseases
5	esv1847869	chr10:96848203-96864595	Enhancers Weak transcription	n/a	n/a	inside rSNPs	diseases
6	nsv1043332	chr10:96851448-96865289	Weak transcription Enhancers	n/a	n/a	inside rSNPs	diseases
7	nsv1040153	chr10:96851448-96869051	Enhancers Weak transcription	n/a	n/a	inside rSNPs	diseases
8	nsv1041915	chr10:96851448-96869694	Weak transcription Enhancers	n/a	n/a	inside rSNPs	diseases
9	nsv1048003	chr10:96853813-96865289	Enhancers Weak transcription	n/a	n/a	inside rSNPs	diseases
10	nsv1042615	chr10:96855366-96869094	Enhancers Weak transcription	n/a	n/a	inside rSNPs	diseases
11	nsv1043378	chr10:96855366-96876009	Enhancers Weak transcription Flanking Active TSS	n/a	n/a	inside rSNPs	diseases

No data

Chromatin state (count:3 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr10:96855600-96856000	Enhancers	Gastric	stomach
2	chr10:96855800-96856400	Enhancers	Fetal Intestine Large	intestine
3	chr10:96855800-96856400	Enhancers	Rectal Mucosa Donor 31	rectum

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