Variant report

Variant	rs11226657
Chromosome Location	chr11:105060775-105060776
allele	A/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 112 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:101)

rs_ID	r²[population]
rs1023953	0.82[ASN][1000 genomes]
rs1023954	0.95[EUR][1000 genomes];0.95[ASN][1000 genomes]
rs10895776	0.82[ASN][1000 genomes]
rs10895778	0.90[EUR][1000 genomes];0.83[ASN][1000 genomes]
rs10895779	0.94[ASN][1000 genomes]
rs10895780	0.82[ASN][1000 genomes]
rs10895781	0.84[ASN][1000 genomes]
rs10895785	0.95[ASN][1000 genomes]
rs10895787	0.94[ASN][1000 genomes]
rs10895788	0.84[ASN][1000 genomes]
rs10895789	0.84[ASN][1000 genomes]
rs10895790	0.96[ASN][1000 genomes]
rs11226613	0.84[CEU][hapmap];0.86[JPT][hapmap]
rs11226619	0.81[ASN][1000 genomes]
rs11226622	0.94[ASN][1000 genomes]
rs11226624	0.94[ASN][1000 genomes]
rs11226625	0.94[ASN][1000 genomes]
rs11226626	0.94[ASN][1000 genomes]
rs11226627	0.82[ASN][1000 genomes]
rs11226628	0.94[ASN][1000 genomes]
rs11226629	0.82[ASN][1000 genomes]
rs11226630	0.95[EUR][1000 genomes];0.95[ASN][1000 genomes]
rs11226631	0.94[ASN][1000 genomes]
rs11226633	0.95[EUR][1000 genomes];0.95[ASN][1000 genomes]
rs11226635	0.94[ASN][1000 genomes]
rs11226638	0.81[ASN][1000 genomes]
rs11226641	0.95[ASN][1000 genomes]
rs11226642	0.84[ASN][1000 genomes]
rs11226645	0.95[ASN][1000 genomes]
rs11226650	0.80[ASN][1000 genomes]
rs11226653	0.86[AMR][1000 genomes];1.00[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs11226655	0.84[ASN][1000 genomes]
rs12222812	0.94[ASN][1000 genomes]
rs12222898	0.95[EUR][1000 genomes];0.95[ASN][1000 genomes]
rs12226317	0.83[ASN][1000 genomes]
rs1351686	0.84[ASN][1000 genomes]
rs1354319	0.94[ASN][1000 genomes]
rs1354320	0.94[ASN][1000 genomes]
rs1354321	0.94[ASN][1000 genomes]
rs1354323	0.94[ASN][1000 genomes]
rs1393908	0.81[ASN][1000 genomes]
rs1503390	0.81[ASN][1000 genomes]
rs1503392	0.81[ASN][1000 genomes]
rs1503394	0.90[EUR][1000 genomes];0.83[ASN][1000 genomes]
rs1503397	0.94[ASN][1000 genomes]
rs1503398	0.94[ASN][1000 genomes]
rs1503401	0.94[ASN][1000 genomes]
rs1566770	0.82[ASN][1000 genomes]
rs17103763	0.95[EUR][1000 genomes];0.95[ASN][1000 genomes]
rs1842893	0.95[EUR][1000 genomes];0.95[ASN][1000 genomes]
rs1842894	0.94[ASN][1000 genomes]
rs1847297	0.94[ASN][1000 genomes]
rs1905257	0.95[ASN][1000 genomes]
rs1994136	0.82[ASN][1000 genomes]
rs2017680	0.95[EUR][1000 genomes];0.95[ASN][1000 genomes]
rs2089048	0.82[ASN][1000 genomes]
rs2200164	0.82[ASN][1000 genomes]
rs2200165	0.84[ASN][1000 genomes]
rs2200166	0.95[ASN][1000 genomes]
rs2291269	0.91[CHB][hapmap];0.86[JPT][hapmap];0.82[ASN][1000 genomes]
rs2409063	0.84[ASN][1000 genomes]
rs35868202	0.94[ASN][1000 genomes]
rs3926237	0.90[EUR][1000 genomes];0.82[ASN][1000 genomes]
rs4754126	0.84[ASN][1000 genomes]
rs4755082	0.94[ASN][1000 genomes]
rs4755083	0.89[ASN][1000 genomes]
rs4755084	0.94[ASN][1000 genomes]
rs4755085	0.94[ASN][1000 genomes]
rs4755086	0.95[EUR][1000 genomes];0.95[ASN][1000 genomes]
rs4755087	0.82[ASN][1000 genomes]
rs4755088	0.94[ASN][1000 genomes]
rs4755089	0.94[ASN][1000 genomes]
rs4755090	0.94[ASN][1000 genomes]
rs4755091	0.84[ASN][1000 genomes]
rs4755094	0.84[ASN][1000 genomes]
rs4755095	0.85[ASN][1000 genomes]
rs4755096	0.89[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs5002812	0.80[AMR][1000 genomes];0.99[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs56180195	0.82[ASN][1000 genomes]
rs57747660	0.83[AMR][1000 genomes];1.00[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs61891100	0.90[EUR][1000 genomes];0.81[ASN][1000 genomes]
rs61891101	0.90[EUR][1000 genomes];0.83[ASN][1000 genomes]
rs61891102	0.90[EUR][1000 genomes];0.83[ASN][1000 genomes]
rs61891134	0.95[EUR][1000 genomes];0.94[ASN][1000 genomes]
rs61891136	0.94[ASN][1000 genomes]
rs6591111	0.82[ASN][1000 genomes]
rs7113151	0.82[ASN][1000 genomes]
rs764078	0.86[AMR][1000 genomes];0.98[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs7925360	0.94[ASN][1000 genomes]
rs7925579	0.94[ASN][1000 genomes]
rs7934633	0.82[ASN][1000 genomes]
rs7940485	0.83[AMR][1000 genomes];1.00[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs7943658	0.94[ASN][1000 genomes]
rs7943758	0.94[ASN][1000 genomes]
rs7943776	0.94[ASN][1000 genomes]
rs7943892	0.82[ASN][1000 genomes]
rs7948306	0.94[ASN][1000 genomes]
rs7948428	0.94[ASN][1000 genomes]
rs7952721	0.82[ASN][1000 genomes]
rs995241	0.94[ASN][1000 genomes]
rs995242	0.94[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	nsv531430	chr11:104380924-105194452	Genic enhancers Flanking Active TSS Enhancers Weak transcription ZNF genes & repeats Active TSS Strong transcription Transcr. at gene 5' and 3' Bivalent Enhancer Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	18 gene(s)	inside rSNPs	diseases
2	nsv468862	chr11:104774014-105243371	Weak transcription Enhancers Flanking Active TSS Active TSS Strong transcription Genic enhancers ZNF genes & repeats Transcr. at gene 5' and 3' Bivalent/Poised TSS Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	15 gene(s)	inside rSNPs	diseases
3	nsv556218	chr11:104774014-105243371	Weak transcription Flanking Active TSS Enhancers Active TSS Strong transcription Genic enhancers ZNF genes & repeats Transcr. at gene 5' and 3' Bivalent/Poised TSS Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	15 gene(s)	inside rSNPs	diseases
4	nsv1044970	chr11:104809246-105225032	Enhancers Active TSS Weak transcription Flanking Active TSS Strong transcription Genic enhancers Transcr. at gene 5' and 3' ZNF genes & repeats Bivalent/Poised TSS Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	13 gene(s)	inside rSNPs	diseases
5	nsv541160	chr11:104809246-105225032	Enhancers Active TSS Weak transcription Flanking Active TSS Genic enhancers Strong transcription ZNF genes & repeats Transcr. at gene 5' and 3' Bivalent Enhancer Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	13 gene(s)	inside rSNPs	diseases
6	nsv949337	chr11:104950007-105510193	Enhancers Bivalent Enhancer Weak transcription Active TSS Flanking Active TSS Flanking Bivalent TSS/Enh Bivalent/Poised TSS Strong transcription ZNF genes & repeats Genic enhancers Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	10 gene(s)	inside rSNPs	diseases
7	nsv528789	chr11:105014564-105133046	Enhancers Weak transcription Flanking Active TSS Active TSS ZNF genes & repeats Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA	4 gene(s)	inside rSNPs	diseases
8	nsv1045900	chr11:105015999-105138877	Enhancers Weak transcription Flanking Active TSS Active TSS ZNF genes & repeats Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA	3 gene(s)	inside rSNPs	diseases
9	nsv556220	chr11:105042650-105112018	Weak transcription Enhancers Flanking Active TSS Active TSS Bivalent Enhancer ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA	1 gene(s)	inside rSNPs	diseases
10	esv2762942	chr11:105044258-105066898	Enhancers Weak transcription Flanking Active TSS ZNF genes & repeats Active TSS	TF binding region Chromatin interactive region lncRNA	1 gene(s)	inside rSNPs	diseases
11	nsv442242	chr11:105049805-105066898	Enhancers Weak transcription Flanking Active TSS Active TSS	TF binding region Chromatin interactive region lncRNA	1 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	chr11:105055400-105060800	Weak transcription	Primary hematopoietic stem cells short term culture	blood
2	chr11:105058800-105063400	Weak transcription	HepG2	liver
3	chr11:105059200-105062000	Enhancers	Primary monocytes fromperipheralblood	blood
4	chr11:105059200-105062000	Enhancers	Primary neutrophils fromperipheralblood	blood
5	chr11:105060200-105060800	Enhancers	Primary B cells from cord blood	blood
6	chr11:105060600-105061400	Flanking Active TSS	Monocytes-CD14+_RO01746	blood

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