Variant report

Variant	rs12271238
Chromosome Location	chr11:67338507-67338508
allele	A/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 58 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:50)

rs_ID	r²[population]
rs10082595	0.90[AFR][1000 genomes]
rs10896187	0.93[AFR][1000 genomes]
rs11227829	0.93[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs11227843	0.89[AFR][1000 genomes]
rs11227847	0.91[AFR][1000 genomes]
rs11227853	0.93[AFR][1000 genomes]
rs11227856	0.93[AFR][1000 genomes]
rs11227858	0.93[AFR][1000 genomes]
rs11227859	0.86[AFR][1000 genomes]
rs11227863	0.88[AFR][1000 genomes]
rs11227864	0.91[AFR][1000 genomes]
rs11227867	0.90[AFR][1000 genomes]
rs11227870	0.84[AFR][1000 genomes]
rs11227872	0.90[AFR][1000 genomes]
rs11501414	0.90[AFR][1000 genomes]
rs12270939	0.94[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs12273818	0.98[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs12274182	1.00[AMR][1000 genomes]
rs12275583	0.94[AFR][1000 genomes]
rs12277603	0.91[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs12279654	0.94[AFR][1000 genomes]
rs12280141	1.00[AMR][1000 genomes]
rs12281959	0.85[AFR][1000 genomes]
rs12283777	0.93[AFR][1000 genomes]
rs12284337	0.81[AFR][1000 genomes]
rs12285190	0.90[AFR][1000 genomes]
rs12285294	0.88[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs12285568	0.93[AFR][1000 genomes]
rs12286629	0.96[AFR][1000 genomes]
rs12287042	0.96[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs12288767	0.93[AFR][1000 genomes]
rs12288862	0.93[AFR][1000 genomes]
rs12288915	0.86[AFR][1000 genomes]
rs12291838	1.00[AMR][1000 genomes]
rs12291861	0.90[AFR][1000 genomes]
rs12292686	1.00[AMR][1000 genomes]
rs12293712	0.81[AFR][1000 genomes]
rs12293788	1.00[AMR][1000 genomes]
rs12295232	0.93[AFR][1000 genomes]
rs12295962	1.00[AMR][1000 genomes]
rs28856416	0.90[AFR][1000 genomes]
rs28894705	0.93[AFR][1000 genomes]
rs4930445	0.81[AFR][1000 genomes]
rs6591248	0.97[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs7102855	0.83[AFR][1000 genomes]
rs7112719	0.90[AFR][1000 genomes]
rs7129806	0.90[AFR][1000 genomes]
rs8191431	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs8191448	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs9651716	0.81[AFR][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:8 , 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	nsv1043037	chr11:67027193-67357425	Enhancers Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3' Flanking Active TSS Strong transcription Genic enhancers Active TSS ZNF genes & repeats Weak transcription Bivalent/Poised TSS Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	213 gene(s)	inside rSNPs	diseases
3	nsv897801	chr11:67033076-67432479	Bivalent Enhancer Enhancers Weak transcription Strong transcription Flanking Active TSS Genic enhancers Active TSS ZNF genes & repeats Bivalent/Poised TSS Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	236 gene(s)	inside rSNPs	diseases
4	nsv897807	chr11:67155210-67414492	Active TSS Bivalent/Poised TSS Strong transcription Genic enhancers Flanking Active TSS Enhancers Weak transcription Bivalent Enhancer Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	176 gene(s)	inside rSNPs	diseases
5	nsv897808	chr11:67155210-67419855	Flanking Active TSS Strong transcription Enhancers Weak transcription Bivalent/Poised TSS Active TSS Flanking Bivalent TSS/Enh Bivalent Enhancer Genic enhancers Transcr. at gene 5' and 3' ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	176 gene(s)	inside rSNPs	diseases
6	nsv534229	chr11:67164667-67411909	Flanking Active TSS Enhancers Weak transcription Transcr. at gene 5' and 3' Bivalent Enhancer Active TSS Strong transcription Genic enhancers Bivalent/Poised TSS ZNF genes & repeats Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	175 gene(s)	inside rSNPs	diseases
7	esv2422195	chr11:67234322-67626901	Enhancers Strong transcription Bivalent Enhancer Flanking Active TSS Genic enhancers Active TSS Weak transcription Flanking Bivalent TSS/Enh Bivalent/Poised TSS Transcr. at gene 5' and 3' ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	146 gene(s)	inside rSNPs	diseases
8	nsv1041988	chr11:67319916-67749246	Enhancers Weak transcription Bivalent/Poised TSS Active TSS Flanking Active TSS Flanking Bivalent TSS/Enh Genic enhancers Strong transcription ZNF genes & repeats Transcr. at gene 5' and 3' Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	84 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:3 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr11:67332000-67339000	Weak transcription	ES-I3 Cell Line	embryonic stem cell
2	chr11:67332200-67339600	Weak transcription	Hela-S3	cervix
3	chr11:67336400-67345200	Weak transcription	Gastric	stomach

The 2.0 version of rSNPBase

Variant report

Quick Search:

what's new

Quick links