Variant report

Variant	rs9633821
Chromosome Location	chr11:26128320-26128321
allele	C/T
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 114 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:113)

rs_ID	r²[population]
rs10501037	1.00[ASN][1000 genomes]
rs11029120	0.82[ASN][1000 genomes]
rs11029127	1.00[ASN][1000 genomes]
rs11029128	1.00[ASN][1000 genomes]
rs11029130	1.00[ASN][1000 genomes]
rs11029132	1.00[ASN][1000 genomes]
rs11029133	1.00[ASN][1000 genomes]
rs11029136	1.00[ASN][1000 genomes]
rs11029137	1.00[ASN][1000 genomes]
rs11029138	1.00[ASN][1000 genomes]
rs11029139	1.00[ASN][1000 genomes]
rs11029140	0.96[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs11029142	0.96[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs11029143	1.00[ASN][1000 genomes]
rs11029144	0.91[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs11029145	0.87[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs11029146	0.91[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs11029147	0.88[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs11029148	0.96[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs11029149	0.96[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs11029150	0.96[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs11029151	0.96[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs11029152	0.96[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs11029153	0.96[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs11029154	1.00[ASN][1000 genomes]
rs11029155	0.96[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs11029156	0.96[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs11029157	1.00[ASN][1000 genomes]
rs11029158	0.96[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs11029159	0.96[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs11029160	0.96[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs11029161	0.96[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs11029162	0.96[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs11029163	0.96[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs11029164	0.96[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs11029165	0.96[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs11029166	1.00[ASN][1000 genomes]
rs11029167	0.96[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs11029168	0.96[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs11029169	0.96[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs11029170	0.96[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs11029171	0.96[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs11029172	0.96[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs11029173	0.96[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs11029174	0.96[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs11029175	0.96[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs11029176	0.96[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs11029177	1.00[ASN][1000 genomes]
rs11029178	1.00[ASN][1000 genomes]
rs11029183	1.00[ASN][1000 genomes]
rs11029184	1.00[ASN][1000 genomes]
rs11029185	1.00[ASN][1000 genomes]
rs11029188	1.00[EUR][1000 genomes];0.92[ASN][1000 genomes]
rs11029189	1.00[ASN][1000 genomes]
rs11029190	1.00[ASN][1000 genomes]
rs11029191	1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs11029192	1.00[ASN][1000 genomes]
rs11029194	1.00[ASN][1000 genomes]
rs11029195	1.00[ASN][1000 genomes]
rs11029196	1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs11029197	1.00[ASN][1000 genomes]
rs11029198	1.00[ASN][1000 genomes]
rs11029199	1.00[ASN][1000 genomes]
rs11029200	1.00[ASN][1000 genomes]
rs11029201	1.00[ASN][1000 genomes]
rs11029203	1.00[ASN][1000 genomes]
rs11029204	1.00[ASN][1000 genomes]
rs11029205	1.00[ASN][1000 genomes]
rs11029210	1.00[ASN][1000 genomes]
rs11029243	0.82[ASN][1000 genomes]
rs11029244	0.82[ASN][1000 genomes]
rs12222395	0.82[ASN][1000 genomes]
rs12222406	0.82[ASN][1000 genomes]
rs12223917	0.82[ASN][1000 genomes]
rs12224552	1.00[ASN][1000 genomes]
rs1387490	1.00[ASN][1000 genomes]
rs1387491	1.00[ASN][1000 genomes]
rs1387492	1.00[ASN][1000 genomes]
rs1489508	0.88[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs1489509	0.96[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs1489510	0.96[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs1489511	0.96[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs16915262	0.96[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs16915268	0.96[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs2349610	1.00[ASN][1000 genomes]
rs2349611	1.00[ASN][1000 genomes]
rs3926027	0.82[EUR][1000 genomes]
rs4360660	0.96[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs4572089	0.96[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs59456245	1.00[ASN][1000 genomes]
rs61688636	0.96[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs66633054	1.00[ASN][1000 genomes]
rs66648383	1.00[ASN][1000 genomes]
rs66699863	1.00[ASN][1000 genomes]
rs72885762	1.00[ASN][1000 genomes]
rs73435407	0.96[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs73435414	0.96[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs73435415	0.96[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs73435418	0.96[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs73435435	0.96[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs73435438	0.96[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs73435442	0.96[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs73435450	0.96[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs73435451	0.96[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs73435502	1.00[ASN][1000 genomes]
rs7935278	0.96[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs7935406	0.96[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs7938817	0.96[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs7952271	0.96[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs9633820	1.00[ASN][1000 genomes]
rs9633854	1.00[ASN][1000 genomes]
rs9633855	1.00[ASN][1000 genomes]
rs977800	1.00[ASN][1000 genomes]

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:5 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr11:26120000-26130200	Weak transcription	Fetal Lung	lung
2	chr11:26127200-26129400	Enhancers	Primary B cells from peripheral blood	blood
3	chr11:26127400-26128600	Enhancers	GM12878-XiMat	blood
4	chr11:26127800-26129400	Enhancers	Primary B cells from cord blood	blood
5	chr11:26128200-26128400	Enhancers	Foreskin Fibroblast Primary Cells skin01	Skin

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