Variant report

Variant	rs10841789
Chromosome Location	chr12:21467666-21467667
allele	A/C
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 184 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:183)

rs_ID	r²[population]
rs1002552	1.00[ASN][1000 genomes]
rs10444413	1.00[CHB][hapmap];1.00[ASN][1000 genomes]
rs10459074	0.95[CEU][hapmap];0.81[EUR][1000 genomes]
rs10459075	0.95[CEU][hapmap];0.81[EUR][1000 genomes]
rs10743411	0.95[CEU][hapmap]
rs10770796	0.95[CEU][hapmap];0.81[EUR][1000 genomes]
rs10770797	0.95[CEU][hapmap]
rs10841761	1.00[ASN][1000 genomes]
rs10841766	1.00[ASN][1000 genomes]
rs10841767	1.00[CHB][hapmap];1.00[ASN][1000 genomes]
rs10841768	1.00[ASN][1000 genomes]
rs10841784	0.95[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs10841786	1.00[CEU][hapmap];0.84[EUR][1000 genomes]
rs10841787	0.84[EUR][1000 genomes]
rs10841791	0.95[CEU][hapmap];0.81[EUR][1000 genomes]
rs10841794	0.95[CEU][hapmap]
rs10841795	1.00[CHB][hapmap];1.00[ASN][1000 genomes]
rs11045783	1.00[ASN][1000 genomes]
rs11045785	1.00[CHB][hapmap];1.00[ASN][1000 genomes]
rs11045786	1.00[CHB][hapmap];1.00[ASN][1000 genomes]
rs11045787	1.00[CHB][hapmap];1.00[ASN][1000 genomes]
rs11045796	1.00[ASN][1000 genomes]
rs11045797	1.00[CHB][hapmap];1.00[ASN][1000 genomes]
rs11045798	1.00[ASN][1000 genomes]
rs11045799	1.00[ASN][1000 genomes]
rs11045801	1.00[ASN][1000 genomes]
rs11045803	1.00[ASN][1000 genomes]
rs11045805	1.00[CHB][hapmap];1.00[ASN][1000 genomes]
rs11045806	1.00[ASN][1000 genomes]
rs11045807	1.00[ASN][1000 genomes]
rs11045813	1.00[CHB][hapmap];1.00[ASN][1000 genomes]
rs11045816	1.00[CHB][hapmap];1.00[ASN][1000 genomes]
rs11045818	1.00[CHB][hapmap];1.00[ASN][1000 genomes]
rs11045819	1.00[CHB][hapmap];1.00[ASN][1000 genomes]
rs11045820	1.00[CHB][hapmap];1.00[ASN][1000 genomes]
rs11045821	1.00[CHB][hapmap];1.00[ASN][1000 genomes]
rs11045823	1.00[CHB][hapmap];1.00[ASN][1000 genomes]
rs11045824	1.00[CHB][hapmap];1.00[ASN][1000 genomes]
rs11045825	1.00[CHB][hapmap];1.00[ASN][1000 genomes]
rs11045831	1.00[ASN][1000 genomes]
rs11045832	1.00[ASN][1000 genomes]
rs11045843	1.00[ASN][1000 genomes]
rs11045856	1.00[ASN][1000 genomes]
rs11045858	1.00[ASN][1000 genomes]
rs11045862	1.00[ASN][1000 genomes]
rs11045863	1.00[CHB][hapmap];1.00[ASN][1000 genomes]
rs11045870	1.00[CHB][hapmap];1.00[ASN][1000 genomes]
rs11045871	1.00[CHB][hapmap];1.00[ASN][1000 genomes]
rs11045872	1.00[CHB][hapmap];1.00[ASN][1000 genomes]
rs11045873	1.00[ASN][1000 genomes]
rs11045874	1.00[ASN][1000 genomes]
rs11045884	1.00[CHB][hapmap];1.00[ASN][1000 genomes]
rs11045887	1.00[CHB][hapmap];1.00[ASN][1000 genomes]
rs11045891	1.00[CHB][hapmap];1.00[ASN][1000 genomes]
rs11045892	1.00[ASN][1000 genomes]
rs11045893	1.00[ASN][1000 genomes]
rs11045897	1.00[ASN][1000 genomes]
rs11045916	1.00[ASN][1000 genomes]
rs11045917	1.00[ASN][1000 genomes]
rs11045918	1.00[CHB][hapmap];1.00[ASN][1000 genomes]
rs11045923	0.95[CEU][hapmap]
rs11045928	1.00[ASN][1000 genomes]
rs11045930	1.00[CEU][hapmap];0.81[AMR][1000 genomes];0.96[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs11045942	1.00[CHB][hapmap];1.00[ASN][1000 genomes]
rs11045946	1.00[CHB][hapmap];1.00[ASN][1000 genomes]
rs11045952	1.00[CHB][hapmap];1.00[ASN][1000 genomes]
rs11045953	1.00[CHB][hapmap];1.00[ASN][1000 genomes]
rs11045956	1.00[CHB][hapmap];1.00[ASN][1000 genomes]
rs11045957	1.00[CHB][hapmap];1.00[ASN][1000 genomes]
rs11045958	1.00[CHB][hapmap];1.00[ASN][1000 genomes]
rs11045960	1.00[CHB][hapmap];1.00[ASN][1000 genomes]
rs11045961	1.00[CHB][hapmap];1.00[ASN][1000 genomes]
rs11045972	1.00[CHB][hapmap];1.00[ASN][1000 genomes]
rs11045974	0.95[CEU][hapmap];0.81[EUR][1000 genomes]
rs11045975	1.00[CEU][hapmap];0.81[EUR][1000 genomes]
rs11045976	0.81[EUR][1000 genomes]
rs11045978	1.00[CHB][hapmap];1.00[ASN][1000 genomes]
rs11045980	0.95[CEU][hapmap]
rs11045981	1.00[ASN][1000 genomes]
rs11494720	1.00[ASN][1000 genomes]
rs11513226	1.00[ASN][1000 genomes]
rs11513228	1.00[ASN][1000 genomes]
rs11513411	1.00[CHB][hapmap];1.00[ASN][1000 genomes]
rs11522782	1.00[ASN][1000 genomes]
rs12231212	0.95[CEU][hapmap]
rs12307908	0.81[AMR][1000 genomes];0.95[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs12311451	1.00[ASN][1000 genomes]
rs12318689	1.00[CHB][hapmap]
rs12367829	1.00[ASN][1000 genomes]
rs12368356	1.00[ASN][1000 genomes]
rs12368481	1.00[ASN][1000 genomes]
rs12370842	1.00[ASN][1000 genomes]
rs12371570	1.00[ASN][1000 genomes]
rs12371691	1.00[ASN][1000 genomes]
rs12372124	1.00[CHB][hapmap];1.00[ASN][1000 genomes]
rs12812279	1.00[CHB][hapmap];1.00[ASN][1000 genomes]
rs12814646	1.00[ASN][1000 genomes]
rs12815795	1.00[ASN][1000 genomes]
rs12819994	1.00[ASN][1000 genomes]
rs12820529	1.00[ASN][1000 genomes]
rs12821068	1.00[ASN][1000 genomes]
rs12821228	1.00[ASN][1000 genomes]
rs12821721	1.00[ASN][1000 genomes]
rs12829704	1.00[CHB][hapmap];1.00[ASN][1000 genomes]
rs12830545	1.00[ASN][1000 genomes]
rs1564367	1.00[ASN][1000 genomes]
rs1564369	1.00[ASN][1000 genomes]
rs17328763	1.00[CHB][hapmap]
rs17329885	1.00[CHB][hapmap];1.00[ASN][1000 genomes]
rs2169969	1.00[CHB][hapmap];1.00[ASN][1000 genomes]
rs2199684	1.00[CHB][hapmap];1.00[ASN][1000 genomes]
rs2199686	1.00[ASN][1000 genomes]
rs2199687	0.84[AMR][1000 genomes];0.96[EUR][1000 genomes]
rs2306231	0.91[CEU][hapmap]
rs2417971	1.00[CEU][hapmap];0.83[EUR][1000 genomes]
rs2417972	0.81[AMR][1000 genomes];0.96[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs28802276	1.00[ASN][1000 genomes]
rs2900480	1.00[CHB][hapmap];1.00[ASN][1000 genomes]
rs34022980	1.00[ASN][1000 genomes]
rs34111581	1.00[ASN][1000 genomes]
rs34211424	1.00[ASN][1000 genomes]
rs34249976	0.98[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs34632551	1.00[ASN][1000 genomes]
rs34888642	1.00[ASN][1000 genomes]
rs35157563	1.00[ASN][1000 genomes]
rs35236625	1.00[ASN][1000 genomes]
rs35406304	1.00[ASN][1000 genomes]
rs35462387	1.00[ASN][1000 genomes]
rs35642680	1.00[ASN][1000 genomes]
rs35736956	1.00[ASN][1000 genomes]
rs35901590	1.00[ASN][1000 genomes]
rs35928112	1.00[ASN][1000 genomes]
rs3794320	1.00[ASN][1000 genomes]
rs4115170	0.95[CEU][hapmap]
rs4148977	0.81[EUR][1000 genomes]
rs4148978	0.81[EUR][1000 genomes]
rs4148984	0.95[CEU][hapmap]
rs4148986	0.95[CEU][hapmap]
rs4148987	0.95[CEU][hapmap]
rs4148988	0.95[CEU][hapmap];0.83[EUR][1000 genomes]
rs4148989	0.95[CEU][hapmap]
rs4148990	0.95[CEU][hapmap]
rs4148991	0.95[CEU][hapmap]
rs4148992	0.95[CEU][hapmap]
rs4148993	0.95[CEU][hapmap];0.86[EUR][1000 genomes]
rs4337089	1.00[ASN][1000 genomes]
rs4381410	1.00[ASN][1000 genomes]
rs4442593	1.00[ASN][1000 genomes]
rs55720923	1.00[ASN][1000 genomes]
rs55773124	1.00[ASN][1000 genomes]
rs55820200	1.00[ASN][1000 genomes]
rs56164184	1.00[ASN][1000 genomes]
rs6487215	1.00[ASN][1000 genomes]
rs6487216	0.95[CEU][hapmap]
rs66777941	1.00[ASN][1000 genomes]
rs7137060	1.00[ASN][1000 genomes]
rs71446755	1.00[ASN][1000 genomes]
rs71446757	1.00[ASN][1000 genomes]
rs71446760	1.00[ASN][1000 genomes]
rs71446761	1.00[ASN][1000 genomes]
rs71446762	1.00[ASN][1000 genomes]
rs71446763	1.00[ASN][1000 genomes]
rs7296472	0.81[EUR][1000 genomes]
rs7305911	0.86[EUR][1000 genomes]
rs7313671	0.95[CEU][hapmap];0.81[EUR][1000 genomes]
rs7485550	1.00[ASN][1000 genomes]
rs7957203	0.95[CEU][hapmap]
rs7957274	1.00[ASN][1000 genomes]
rs7960384	1.00[ASN][1000 genomes]
rs7960688	1.00[ASN][1000 genomes]
rs7962263	1.00[CEU][hapmap];1.00[CHB][hapmap];0.82[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs7962919	0.82[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs7963398	0.95[CEU][hapmap];0.81[EUR][1000 genomes]
rs7965059	1.00[ASN][1000 genomes]
rs7967303	1.00[CHB][hapmap];1.00[ASN][1000 genomes]
rs7967403	1.00[CHB][hapmap];1.00[ASN][1000 genomes]
rs7967935	0.95[CEU][hapmap]
rs7968331	0.95[CEU][hapmap]
rs7974575	1.00[YRI][hapmap]
rs7977197	1.00[ASN][1000 genomes]
rs7977517	0.95[CEU][hapmap]
rs7978322	1.00[CHB][hapmap];1.00[ASN][1000 genomes]
rs7978981	0.95[CEU][hapmap]

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

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv557735	chr12:21443282-21538957	Enhancers Weak transcription Flanking Active TSS ZNF genes & repeats Active TSS Strong transcription Genic enhancers Bivalent/Poised TSS Bivalent Enhancer	TF binding region CpG island Chromatin interactive region	4 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:6 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr12:21416200-21473600	Weak transcription	Brain Inferior Temporal Lobe	brain
2	chr12:21461000-21473800	Weak transcription	Brain Angular Gyrus	brain
3	chr12:21463800-21468000	Weak transcription	Brain Dorsolateral Prefrontal Cortex	brain
4	chr12:21464800-21473400	Weak transcription	Brain Hippocampus Middle	brain
5	chr12:21467200-21468000	Enhancers	K562	blood
6	chr12:21467600-21468000	Enhancers	Brain Substantia Nigra	brain

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