Variant report

Variant	rs11227681
Chromosome Location	chr11:66851583-66851584
allele	A/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 39 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:37)

rs_ID	r²[population]
rs10128545	1.00[AMR][1000 genomes]
rs11227704	0.95[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs11227705	0.84[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs11227708	1.00[AMR][1000 genomes]
rs11227734	1.00[AMR][1000 genomes]
rs11227739	0.82[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs11227741	0.82[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs11227749	0.89[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs11227754	0.85[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs11501507	0.83[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs12270253	0.90[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs12274690	1.00[AMR][1000 genomes]
rs12274763	1.00[AMR][1000 genomes]
rs12275826	0.87[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs12282634	0.83[AMR][1000 genomes]
rs12282851	0.92[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs12283056	1.00[AMR][1000 genomes]
rs12284445	1.00[AMR][1000 genomes]
rs12285582	0.89[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs12286106	0.83[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs12286762	1.00[AMR][1000 genomes]
rs12287003	0.88[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs12287355	0.88[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs12287649	0.89[AFR][1000 genomes]
rs12290300	1.00[AMR][1000 genomes]
rs12293258	0.95[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs12294777	1.00[AMR][1000 genomes]
rs3730309	0.86[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs3730310	1.00[AMR][1000 genomes]
rs4370946	1.00[AMR][1000 genomes]
rs61758504	1.00[AMR][1000 genomes]
rs7111472	0.97[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs7128315	0.80[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs7478885	1.00[AMR][1000 genomes]
rs7928575	0.91[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs7945629	1.00[AMR][1000 genomes]
rs948988	1.00[AMR][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:2 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv531397	chr11:66653381-67465721	Active TSS Enhancers Strong transcription Flanking Active TSS Weak transcription Transcr. at gene 5' and 3' Genic enhancers Bivalent Enhancer Bivalent/Poised TSS Flanking Bivalent TSS/Enh ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	271 gene(s)	inside rSNPs	diseases
2	nsv532287	chr11:66784014-67023899	Weak transcription Strong transcription Bivalent Enhancer Enhancers Flanking Active TSS Active TSS Transcr. at gene 5' and 3' Genic enhancers Flanking Bivalent TSS/Enh Bivalent/Poised TSS ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	48 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	chr11:66849600-66852000	Weak transcription	H9 Cell Line	embryonic stem cell
2	chr11:66850200-66851800	Enhancers	Hela-S3	cervix
3	chr11:66850800-66866000	Weak transcription	Right Atrium	heart
4	chr11:66851400-66851600	Enhancers	Foreskin Keratinocyte Primary Cells skin03	Skin
5	chr11:66851400-66851600	Enhancers	A549	lung

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