Variant report

Variant	rs11029199
Chromosome Location	chr11:26130519-26130520
allele	A/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

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	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[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	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[ASN][1000 genomes]
rs11029194	1.00[ASN][1000 genomes]
rs11029195	1.00[ASN][1000 genomes]
rs11029196	1.00[ASN][1000 genomes]
rs11029197	1.00[ASN][1000 genomes]
rs11029198	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	1.00[ASN][1000 genomes]
rs1489509	1.00[ASN][1000 genomes]
rs1489510	1.00[ASN][1000 genomes]
rs1489511	1.00[ASN][1000 genomes]
rs16915262	1.00[ASN][1000 genomes]
rs16915268	1.00[ASN][1000 genomes]
rs2349610	1.00[ASN][1000 genomes]
rs2349611	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]
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	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[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[ASN][1000 genomes]
rs977800	1.00[ASN][1000 genomes]

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

Chromatin state (count:7 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr11:26128600-26133600	Weak transcription	GM12878-XiMat	blood
2	chr11:26129400-26133800	Weak transcription	Primary B cells from peripheral blood	blood
3	chr11:26129600-26130800	Enhancers	Foreskin Fibroblast Primary Cells skin01	Skin
4	chr11:26129600-26131600	Enhancers	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
5	chr11:26130200-26132800	Enhancers	Fetal Lung	lung
6	chr11:26130400-26130600	Enhancers	Colon Smooth Muscle	Colon
7	chr11:26130400-26130800	Enhancers	Ovary	ovary

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dbSNP/dbVar ID: rs12345 /nsv7879
a single nucleotide as 0-based coordinates: chr1:12345
chromosomal regions: chr1:12345-34567

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