Variant report

Variant	rs34497705
Chromosome Location	chr10:55325295-55325296
allele	CA/TG
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 124 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:116)

rs_ID	r²[population]
rs11527272	0.83[EUR][1000 genomes]
rs11527477	0.84[EUR][1000 genomes]
rs11527478	0.84[EUR][1000 genomes]
rs1762109	0.84[EUR][1000 genomes]
rs2484208	0.83[EUR][1000 genomes]
rs2484209	0.81[EUR][1000 genomes]
rs2632535	0.83[EUR][1000 genomes]
rs2931565	0.82[AMR][1000 genomes];0.85[EUR][1000 genomes]
rs2992011	0.82[AMR][1000 genomes];0.85[EUR][1000 genomes]
rs34095257	0.83[EUR][1000 genomes]
rs34632242	0.83[EUR][1000 genomes]
rs351799	0.81[AMR][1000 genomes];0.84[EUR][1000 genomes]
rs351800	0.83[AMR][1000 genomes];0.86[EUR][1000 genomes]
rs351801	0.80[EUR][1000 genomes]
rs351802	0.82[EUR][1000 genomes]
rs351803	0.82[EUR][1000 genomes]
rs35424889	0.83[EUR][1000 genomes]
rs35891588	0.82[EUR][1000 genomes]
rs36065206	0.91[AMR][1000 genomes];0.96[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs364694	0.83[EUR][1000 genomes]
rs365966	0.83[EUR][1000 genomes]
rs368110	0.84[EUR][1000 genomes]
rs368703	0.84[EUR][1000 genomes]
rs371543	0.82[EUR][1000 genomes]
rs372338	0.86[AMR][1000 genomes];0.89[EUR][1000 genomes]
rs374009	0.84[EUR][1000 genomes]
rs374891	0.83[EUR][1000 genomes]
rs376278	0.83[EUR][1000 genomes]
rs379033	0.84[EUR][1000 genomes]
rs380989	0.84[EUR][1000 genomes]
rs381979	0.84[EUR][1000 genomes]
rs382870	0.82[EUR][1000 genomes]
rs386060	0.83[EUR][1000 genomes]
rs389244	0.82[EUR][1000 genomes]
rs392293	0.83[EUR][1000 genomes]
rs392668	0.83[EUR][1000 genomes]
rs394770	0.83[EUR][1000 genomes]
rs394942	0.82[EUR][1000 genomes]
rs395825	0.83[EUR][1000 genomes]
rs396374	0.82[EUR][1000 genomes]
rs397301	0.82[EUR][1000 genomes]
rs398169	0.85[EUR][1000 genomes];0.82[ASN][1000 genomes]
rs399032	0.83[EUR][1000 genomes]
rs399409	0.84[EUR][1000 genomes]
rs399606	0.82[EUR][1000 genomes]
rs401333	0.83[EUR][1000 genomes]
rs401407	0.84[EUR][1000 genomes]
rs404593	0.84[EUR][1000 genomes]
rs407646	0.82[EUR][1000 genomes]
rs409001	0.82[EUR][1000 genomes]
rs409369	0.84[EUR][1000 genomes]
rs409814	0.84[EUR][1000 genomes]
rs413137	0.82[EUR][1000 genomes]
rs414849	0.83[EUR][1000 genomes]
rs418047	0.84[EUR][1000 genomes]
rs420314	0.83[EUR][1000 genomes]
rs423146	0.83[EUR][1000 genomes]
rs423384	0.82[EUR][1000 genomes]
rs423806	0.82[EUR][1000 genomes]
rs425467	0.83[EUR][1000 genomes]
rs426290	0.86[EUR][1000 genomes]
rs427201	0.84[EUR][1000 genomes]
rs427372	0.84[EUR][1000 genomes]
rs427506	0.83[EUR][1000 genomes]
rs428127	0.83[EUR][1000 genomes]
rs428467	0.82[EUR][1000 genomes]
rs428563	0.82[EUR][1000 genomes]
rs430495	0.82[EUR][1000 genomes]
rs433574	0.84[EUR][1000 genomes]
rs433582	0.84[EUR][1000 genomes]
rs437390	0.83[EUR][1000 genomes]
rs440743	0.82[EUR][1000 genomes]
rs441336	0.84[EUR][1000 genomes]
rs443931	0.83[EUR][1000 genomes]
rs444728	0.80[AMR][1000 genomes];0.87[EUR][1000 genomes]
rs445488	0.82[EUR][1000 genomes]
rs447549	0.84[EUR][1000 genomes]
rs450516	0.82[EUR][1000 genomes]
rs451452	0.83[EUR][1000 genomes]
rs451485	0.82[EUR][1000 genomes]
rs451607	0.83[EUR][1000 genomes]
rs453158	0.82[EUR][1000 genomes]
rs454270	0.83[EUR][1000 genomes]
rs455078	0.83[EUR][1000 genomes]
rs4622165	0.93[AMR][1000 genomes];0.99[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs4628595	0.83[EUR][1000 genomes]
rs596456	0.83[EUR][1000 genomes]
rs598529	0.82[EUR][1000 genomes]
rs598536	0.82[EUR][1000 genomes]
rs607228	0.83[EUR][1000 genomes]
rs607276	0.91[AMR][1000 genomes];0.97[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs609908	0.83[EUR][1000 genomes]
rs610251	0.83[EUR][1000 genomes]
rs61859905	0.83[EUR][1000 genomes]
rs61859906	0.82[EUR][1000 genomes]
rs61859907	0.82[EUR][1000 genomes]
rs61859908	0.82[EUR][1000 genomes]
rs636340	0.83[EUR][1000 genomes]
rs637714	0.84[EUR][1000 genomes]
rs6415918	0.82[EUR][1000 genomes]
rs6481015	0.83[AMR][1000 genomes];0.86[EUR][1000 genomes]
rs6481016	0.82[EUR][1000 genomes]
rs658983	0.82[EUR][1000 genomes]
rs659014	0.83[EUR][1000 genomes]
rs659421	0.84[EUR][1000 genomes]
rs663624	0.83[EUR][1000 genomes]
rs665850	0.83[EUR][1000 genomes]
rs66668165	0.82[EUR][1000 genomes]
rs66678299	0.83[EUR][1000 genomes]
rs668434	0.82[EUR][1000 genomes]
rs674159	0.84[EUR][1000 genomes]
rs678459	0.82[EUR][1000 genomes]
rs689581	0.83[EUR][1000 genomes]
rs7075007	0.81[EUR][1000 genomes]
rs7898607	0.83[EUR][1000 genomes]
rs7898708	0.81[EUR][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:8 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	esv2752952	chr10:54900994-55497594	Weak transcription ZNF genes & repeats Enhancers Flanking Active TSS Bivalent Enhancer Active TSS Strong transcription	TF binding region CpG island Chromatin interactive region lncRNA	4 gene(s)	inside rSNPs	diseases
2	nsv1044282	chr10:55186501-55516392	Enhancers Weak transcription ZNF genes & repeats Active TSS Flanking Active TSS Strong transcription	TF binding region CpG island Chromatin interactive region	1 gene(s)	inside rSNPs	diseases
3	nsv540631	chr10:55186501-55516392	Enhancers Weak transcription ZNF genes & repeats Flanking Active TSS Strong transcription Active TSS	TF binding region CpG island Chromatin interactive region	1 gene(s)	inside rSNPs	diseases
4	nsv1043501	chr10:55186701-55516253	Weak transcription Enhancers Flanking Active TSS ZNF genes & repeats Strong transcription Active TSS	TF binding region CpG island Chromatin interactive region	1 gene(s)	inside rSNPs	diseases
5	nsv540632	chr10:55186701-55516253	Enhancers Weak transcription ZNF genes & repeats Active TSS Flanking Active TSS Strong transcription	TF binding region CpG island Chromatin interactive region	1 gene(s)	inside rSNPs	diseases
6	nsv1050323	chr10:55190079-55546575	Weak transcription ZNF genes & repeats Enhancers Active TSS Strong transcription Flanking Active TSS	TF binding region CpG island Chromatin interactive region lncRNA	2 gene(s)	inside rSNPs	diseases
7	esv20996	chr10:55318849-55328766	Weak transcription Enhancers ZNF genes & repeats	Chromatin interactive region	n/a	inside rSNPs	diseases
8	nsv825388	chr10:55320235-55328054	Weak transcription ZNF genes & repeats Enhancers	Chromatin interactive region	n/a	inside rSNPs	diseases

No data

Chromatin state (count:2 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr10:55324800-55334000	Weak transcription	ES-UCSF4 Cell Line	embryonic stem cell
2	chr10:55325200-55325400	Weak transcription	iPS-15b Cell Line	embryonic stem cell

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