Variant report

Variant	rs11029184
Chromosome Location	chr11:26123872-26123873
allele	C/T
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 147 )
Associated
traits (count: 0)

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

rs_ID	r²[population]
rs10501037	1.00[ASN][1000 genomes]
rs10734366	1.00[CHB][hapmap]
rs10742127	1.00[CHB][hapmap]
rs10742128	1.00[CHB][hapmap]
rs10834897	1.00[CHB][hapmap]
rs10834898	1.00[CHB][hapmap]
rs10834914	0.84[EUR][1000 genomes]
rs11029102	0.84[EUR][1000 genomes]
rs11029103	0.84[EUR][1000 genomes]
rs11029104	0.92[EUR][1000 genomes]
rs11029106	0.92[EUR][1000 genomes]
rs11029114	1.00[CHB][hapmap]
rs11029115	0.92[EUR][1000 genomes]
rs11029120	0.82[ASN][1000 genomes]
rs11029124	0.92[EUR][1000 genomes]
rs11029127	1.00[ASN][1000 genomes]
rs11029128	1.00[ASN][1000 genomes]
rs11029130	1.00[ASN][1000 genomes]
rs11029132	0.92[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs11029133	1.00[ASN][1000 genomes]
rs11029136	0.92[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs11029137	1.00[ASN][1000 genomes]
rs11029138	0.92[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs11029139	0.92[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs11029140	1.00[ASN][1000 genomes]
rs11029142	1.00[ASN][1000 genomes]
rs11029143	1.00[ASN][1000 genomes]
rs11029144	1.00[ASN][1000 genomes]
rs11029145	1.00[ASN][1000 genomes]
rs11029146	1.00[ASN][1000 genomes]
rs11029147	1.00[ASN][1000 genomes]
rs11029148	1.00[ASN][1000 genomes]
rs11029149	1.00[ASN][1000 genomes]
rs11029150	1.00[ASN][1000 genomes]
rs11029151	1.00[ASN][1000 genomes]
rs11029152	1.00[ASN][1000 genomes]
rs11029153	1.00[ASN][1000 genomes]
rs11029154	1.00[ASN][1000 genomes]
rs11029155	1.00[ASN][1000 genomes]
rs11029156	1.00[ASN][1000 genomes]
rs11029157	1.00[ASN][1000 genomes]
rs11029158	1.00[ASN][1000 genomes]
rs11029159	1.00[ASN][1000 genomes]
rs11029160	1.00[ASN][1000 genomes]
rs11029161	1.00[ASN][1000 genomes]
rs11029162	1.00[ASN][1000 genomes]
rs11029163	1.00[ASN][1000 genomes]
rs11029164	1.00[ASN][1000 genomes]
rs11029165	1.00[ASN][1000 genomes]
rs11029166	1.00[ASN][1000 genomes]
rs11029167	1.00[ASN][1000 genomes]
rs11029168	1.00[ASN][1000 genomes]
rs11029169	1.00[ASN][1000 genomes]
rs11029170	1.00[ASN][1000 genomes]
rs11029171	1.00[ASN][1000 genomes]
rs11029172	1.00[ASN][1000 genomes]
rs11029173	1.00[ASN][1000 genomes]
rs11029174	1.00[ASN][1000 genomes]
rs11029175	1.00[ASN][1000 genomes]
rs11029176	1.00[ASN][1000 genomes]
rs11029177	1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs11029178	1.00[ASN][1000 genomes]
rs11029183	1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs11029185	1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs11029188	0.92[ASN][1000 genomes]
rs11029189	1.00[ASN][1000 genomes]
rs11029190	1.00[ASN][1000 genomes]
rs11029191	1.00[ASN][1000 genomes]
rs11029192	1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs11029194	1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs11029195	1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs11029196	1.00[ASN][1000 genomes]
rs11029197	1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs11029198	1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs11029199	1.00[ASN][1000 genomes]
rs11029200	1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs11029201	1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs11029203	1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs11029204	1.00[ASN][1000 genomes]
rs11029205	1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs11029210	1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs11029243	0.84[EUR][1000 genomes];0.82[ASN][1000 genomes]
rs11029244	0.84[EUR][1000 genomes];0.82[ASN][1000 genomes]
rs11029249	0.84[EUR][1000 genomes]
rs11029252	0.84[EUR][1000 genomes]
rs11029370	1.00[CEU][hapmap]
rs11029371	1.00[CEU][hapmap]
rs12222395	0.92[EUR][1000 genomes];0.82[ASN][1000 genomes]
rs12222406	1.00[EUR][1000 genomes];0.82[ASN][1000 genomes]
rs12223917	1.00[EUR][1000 genomes];0.82[ASN][1000 genomes]
rs12224552	0.92[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs12225865	1.00[CHB][hapmap]
rs1387490	1.00[ASN][1000 genomes]
rs1387491	0.92[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs1387492	0.92[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs1387503	1.00[CHB][hapmap]
rs1387507	1.00[CHB][hapmap]
rs1489508	1.00[ASN][1000 genomes]
rs1489509	1.00[ASN][1000 genomes]
rs1489510	1.00[ASN][1000 genomes]
rs1489511	1.00[ASN][1000 genomes]
rs16915247	0.84[AFR][1000 genomes]
rs16915262	1.00[ASN][1000 genomes]
rs16915268	1.00[ASN][1000 genomes]
rs16915272	0.84[AFR][1000 genomes]
rs2349610	0.92[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs2349611	0.85[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs4360660	1.00[ASN][1000 genomes]
rs4572089	1.00[ASN][1000 genomes]
rs59456245	1.00[ASN][1000 genomes]
rs61688636	1.00[ASN][1000 genomes]
rs6484193	1.00[CHB][hapmap]
rs66633054	1.00[ASN][1000 genomes]
rs66648383	1.00[ASN][1000 genomes]
rs66699863	1.00[ASN][1000 genomes]
rs7101817	1.00[CHB][hapmap]
rs7105188	1.00[CHB][hapmap]
rs7105339	1.00[CHB][hapmap]
rs7115939	1.00[CHB][hapmap]
rs7116083	1.00[CHB][hapmap]
rs7119696	1.00[CHB][hapmap]
rs7123678	1.00[CHB][hapmap]
rs72885762	1.00[ASN][1000 genomes]
rs73435407	1.00[ASN][1000 genomes]
rs73435414	1.00[ASN][1000 genomes]
rs73435415	1.00[ASN][1000 genomes]
rs73435418	1.00[ASN][1000 genomes]
rs73435435	1.00[ASN][1000 genomes]
rs73435438	1.00[ASN][1000 genomes]
rs73435442	1.00[ASN][1000 genomes]
rs73435450	1.00[ASN][1000 genomes]
rs73435451	1.00[ASN][1000 genomes]
rs73435502	1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs7935278	1.00[ASN][1000 genomes]
rs7935406	1.00[ASN][1000 genomes]
rs7938817	1.00[ASN][1000 genomes]
rs7952271	1.00[ASN][1000 genomes]
rs9633820	1.00[ASN][1000 genomes]
rs9633821	1.00[ASN][1000 genomes]
rs9633854	1.00[ASN][1000 genomes]
rs9633855	1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs977800	0.92[AFR][1000 genomes];0.92[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs977801	0.92[AFR][1000 genomes]
rs988513	1.00[CHB][hapmap]
rs988514	1.00[CHB][hapmap]
rs988516	1.00[CHB][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	esv2760599	chr11:25186984-26159450	Enhancers Flanking Active TSS Weak transcription ZNF genes & repeats Genic enhancers Active TSS Bivalent Enhancer Flanking Bivalent TSS/Enh Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA	6 gene(s)	inside rSNPs	diseases

No data

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

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr11:26120000-26130200	Weak transcription	Fetal Lung	lung
2	chr11:26121200-26124000	Weak transcription	Primary B cells from cord blood	blood

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