Variant report

Variant	rs11823732
Chromosome Location	chr11:84957905-84957906
allele	G/T
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 140 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:136)

rs_ID	r²[population]
rs10501589	1.00[CHB][hapmap];0.94[CHD][hapmap];1.00[JPT][hapmap];0.98[ASN][1000 genomes]
rs10501592	1.00[JPT][hapmap];0.98[ASN][1000 genomes]
rs11821513	0.91[ASN][1000 genomes]
rs11822362	0.91[ASN][1000 genomes]
rs11823560	1.00[CHB][hapmap];0.92[JPT][hapmap]
rs11823978	0.93[ASN][1000 genomes]
rs11825901	0.93[ASN][1000 genomes]
rs11827372	1.00[ASW][hapmap];0.81[CHD][hapmap];1.00[JPT][hapmap];0.93[ASN][1000 genomes]
rs12281150	0.82[CEU][hapmap];1.00[CHD][hapmap];0.86[JPT][hapmap];0.81[ASN][1000 genomes]
rs12788992	0.93[ASW][hapmap];0.94[CHD][hapmap];1.00[GIH][hapmap];1.00[JPT][hapmap];1.00[MEX][hapmap];1.00[TSI][hapmap];0.91[AMR][1000 genomes];0.83[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs1602992	1.00[CHB][hapmap];0.94[CHD][hapmap];0.93[JPT][hapmap];0.89[ASN][1000 genomes]
rs17148016	1.00[CHB][hapmap];0.89[CHD][hapmap];1.00[GIH][hapmap];1.00[JPT][hapmap];0.98[ASN][1000 genomes]
rs17148028	1.00[CHB][hapmap];0.93[JPT][hapmap];0.84[ASN][1000 genomes]
rs17148044	1.00[CHB][hapmap];1.00[JPT][hapmap]
rs17148047	1.00[CHB][hapmap];1.00[CHD][hapmap];1.00[JPT][hapmap]
rs17148049	1.00[CHB][hapmap];0.94[CHD][hapmap];1.00[JPT][hapmap];0.94[ASN][1000 genomes]
rs17148061	1.00[CHB][hapmap];1.00[JPT][hapmap];0.83[YRI][hapmap];0.88[AFR][1000 genomes];0.94[ASN][1000 genomes]
rs17148063	1.00[CHB][hapmap];0.94[CHD][hapmap];1.00[GIH][hapmap];1.00[JPT][hapmap];1.00[TSI][hapmap];1.00[ASN][1000 genomes]
rs17148067	1.00[CHB][hapmap];1.00[JPT][hapmap];0.87[AFR][1000 genomes];0.96[AMR][1000 genomes];0.83[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs17148070	1.00[CHB][hapmap];1.00[JPT][hapmap];0.96[AMR][1000 genomes];0.83[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs17148078	0.93[ASW][hapmap];0.94[CHD][hapmap];1.00[GIH][hapmap];1.00[JPT][hapmap];0.90[LWK][hapmap];1.00[MEX][hapmap];1.00[TSI][hapmap];0.83[YRI][hapmap];0.82[AFR][1000 genomes];0.96[AMR][1000 genomes];0.83[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs17148086	0.93[ASN][1000 genomes]
rs17148090	0.98[ASN][1000 genomes]
rs17159864	0.98[ASN][1000 genomes]
rs17207605	1.00[CHB][hapmap];0.85[JPT][hapmap];0.83[ASN][1000 genomes]
rs17207843	1.00[CHB][hapmap];1.00[JPT][hapmap];0.98[ASN][1000 genomes]
rs17207864	1.00[CHB][hapmap];1.00[JPT][hapmap];1.00[ASN][1000 genomes]
rs17208108	1.00[CHB][hapmap];1.00[JPT][hapmap];0.83[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs17208150	1.00[CHB][hapmap];0.91[JPT][hapmap];0.98[ASN][1000 genomes]
rs17208171	1.00[CHB][hapmap];1.00[JPT][hapmap];0.83[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs17208192	1.00[CHB][hapmap];1.00[JPT][hapmap];0.83[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs17809753	1.00[CHB][hapmap];0.85[JPT][hapmap]
rs17810172	1.00[CHB][hapmap];1.00[CHD][hapmap];1.00[GIH][hapmap];0.93[JPT][hapmap];0.83[TSI][hapmap];0.86[ASN][1000 genomes]
rs17810280	0.92[JPT][hapmap]
rs17810291	1.00[CHB][hapmap];1.00[JPT][hapmap];0.94[ASN][1000 genomes]
rs17810357	1.00[CHB][hapmap];1.00[JPT][hapmap];0.83[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs17810405	1.00[CHB][hapmap];1.00[CHD][hapmap];1.00[GIH][hapmap];1.00[JPT][hapmap];1.00[TSI][hapmap];1.00[ASN][1000 genomes]
rs17810429	1.00[CHB][hapmap];1.00[JPT][hapmap];0.83[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs17810490	0.98[ASN][1000 genomes]
rs17810611	0.85[ASN][1000 genomes]
rs1914371	1.00[CHB][hapmap];1.00[JPT][hapmap];0.85[AFR][1000 genomes];0.94[ASN][1000 genomes]
rs1914372	1.00[CHB][hapmap];1.00[JPT][hapmap];0.85[AFR][1000 genomes];0.96[AMR][1000 genomes];1.00[ASN][1000 genomes]
rs2032410	1.00[CHB][hapmap];1.00[CHD][hapmap];1.00[JPT][hapmap];0.94[ASN][1000 genomes]
rs2036782	0.80[ASN][1000 genomes]
rs2056182	1.00[CHB][hapmap];1.00[JPT][hapmap];0.94[ASN][1000 genomes]
rs2088015	0.98[ASN][1000 genomes]
rs2088016	0.89[ASN][1000 genomes]
rs2088017	1.00[CHB][hapmap];0.94[CHD][hapmap];0.93[JPT][hapmap];0.89[ASN][1000 genomes]
rs2213116	0.96[ASN][1000 genomes]
rs3941173	0.89[ASN][1000 genomes]
rs56306275	0.82[AMR][1000 genomes];0.96[ASN][1000 genomes]
rs57104960	0.96[ASN][1000 genomes]
rs57671189	0.89[ASN][1000 genomes]
rs58028528	0.98[ASN][1000 genomes]
rs58117031	0.85[ASN][1000 genomes]
rs58464081	0.98[ASN][1000 genomes]
rs58515356	0.88[ASN][1000 genomes]
rs58756447	0.94[ASN][1000 genomes]
rs59464672	0.85[ASN][1000 genomes]
rs59583891	0.93[ASN][1000 genomes]
rs59713586	0.85[ASN][1000 genomes]
rs59851854	0.89[ASN][1000 genomes]
rs59869002	0.96[ASN][1000 genomes]
rs60030322	0.89[ASN][1000 genomes]
rs60284674	0.86[ASN][1000 genomes]
rs60360244	1.00[ASN][1000 genomes]
rs60383907	0.98[ASN][1000 genomes]
rs61368496	0.98[ASN][1000 genomes]
rs61697848	0.94[ASN][1000 genomes]
rs6592235	1.00[JPT][hapmap];0.82[AFR][1000 genomes];0.93[ASN][1000 genomes]
rs6592236	1.00[JPT][hapmap];0.82[AFR][1000 genomes];0.93[ASN][1000 genomes]
rs7108893	1.00[CHB][hapmap];1.00[JPT][hapmap]
rs7110155	1.00[CHB][hapmap];0.93[JPT][hapmap];0.89[ASN][1000 genomes]
rs7112335	1.00[CHB][hapmap];1.00[CHD][hapmap];1.00[GIH][hapmap];1.00[JPT][hapmap];1.00[TSI][hapmap]
rs7117010	0.80[ASN][1000 genomes]
rs7129666	1.00[CHB][hapmap];1.00[CHD][hapmap];1.00[GIH][hapmap];1.00[JPT][hapmap];1.00[TSI][hapmap]
rs72945906	0.98[ASN][1000 genomes]
rs72945910	0.98[ASN][1000 genomes]
rs72945914	0.89[ASN][1000 genomes]
rs72945917	0.89[ASN][1000 genomes]
rs72945919	0.98[ASN][1000 genomes]
rs72945920	0.89[ASN][1000 genomes]
rs72945921	0.89[ASN][1000 genomes]
rs72945944	1.00[ASN][1000 genomes]
rs72945948	1.00[ASN][1000 genomes]
rs72945956	0.94[ASN][1000 genomes]
rs72945965	0.94[ASN][1000 genomes]
rs72947961	0.94[ASN][1000 genomes]
rs72947963	0.94[ASN][1000 genomes]
rs72947971	1.00[AMR][1000 genomes];0.83[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs72947974	1.00[ASN][1000 genomes]
rs72947975	0.90[AFR][1000 genomes];0.96[AMR][1000 genomes];1.00[ASN][1000 genomes]
rs72947981	1.00[ASN][1000 genomes]
rs72947999	0.83[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs72950104	0.94[ASN][1000 genomes]
rs72950107	0.98[ASN][1000 genomes]
rs72950109	0.93[ASN][1000 genomes]
rs72950128	0.83[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs72950129	0.83[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs72950131	0.83[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs72950137	0.93[ASN][1000 genomes]
rs72950141	0.96[ASN][1000 genomes]
rs72950152	0.98[ASN][1000 genomes]
rs72950153	0.98[ASN][1000 genomes]
rs72950156	0.83[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs72950157	0.83[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs72950158	0.83[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs72950161	0.83[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs72950165	0.98[ASN][1000 genomes]
rs72950167	0.98[ASN][1000 genomes]
rs72950168	0.98[ASN][1000 genomes]
rs72950169	0.98[ASN][1000 genomes]
rs72950175	0.98[ASN][1000 genomes]
rs72950176	0.98[ASN][1000 genomes]
rs72950181	0.98[ASN][1000 genomes]
rs72950182	0.98[ASN][1000 genomes]
rs72950186	0.96[ASN][1000 genomes]
rs72951917	0.96[ASN][1000 genomes]
rs72951920	0.85[ASN][1000 genomes]
rs72951948	0.82[ASN][1000 genomes]
rs72961528	0.98[ASN][1000 genomes]
rs72961539	0.93[ASN][1000 genomes]
rs72961540	0.94[ASN][1000 genomes]
rs72961550	0.98[ASN][1000 genomes]
rs72961552	0.89[ASN][1000 genomes]
rs72961553	0.98[ASN][1000 genomes]
rs72961554	0.93[ASN][1000 genomes]
rs72961555	0.98[ASN][1000 genomes]
rs72961557	0.98[ASN][1000 genomes]
rs72961558	0.98[ASN][1000 genomes]
rs72961562	0.98[ASN][1000 genomes]
rs72961567	0.89[ASN][1000 genomes]
rs72961570	0.98[ASN][1000 genomes]
rs7924587	0.93[ASN][1000 genomes]
rs7940610	0.88[ASN][1000 genomes]
rs7947098	0.94[ASN][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:4 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv1044370	chr11:84748993-85293233	Enhancers Weak transcription ZNF genes & repeats Active TSS Strong transcription Bivalent/Poised TSS Flanking Bivalent TSS/Enh Flanking Active TSS Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA	22 gene(s)	inside rSNPs	diseases
2	nsv898042	chr11:84877221-84965437	Weak transcription ZNF genes & repeats Enhancers Flanking Active TSS	Chromatin interactive region	n/a	inside rSNPs	diseases
3	nsv898043	chr11:84895033-85148689	Enhancers Active TSS Weak transcription ZNF genes & repeats Flanking Active TSS Strong transcription	TF binding region CpG island Chromatin interactive region lncRNA	3 gene(s)	inside rSNPs	diseases
4	nsv898044	chr11:84895033-85220773	ZNF genes & repeats Flanking Bivalent TSS/Enh Enhancers Weak transcription Active TSS Flanking Active TSS Bivalent Enhancer Strong transcription Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA	20 gene(s)	inside rSNPs	diseases

No data

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

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr11:84954200-84964400	Weak transcription	Psoas Muscle	Psoas

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