Variant report

Variant	rs11050981
Chromosome Location	chr12:30753796-30753797
allele	C/T
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 66 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:65)

rs_ID	r²[population]
rs10431223	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];0.83[ASN][1000 genomes]
rs11050960	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];0.83[ASN][1000 genomes]
rs11050962	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];0.83[ASN][1000 genomes]
rs11050963	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];0.86[ASN][1000 genomes]
rs11050964	0.84[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];0.86[ASN][1000 genomes]
rs11050965	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];0.86[ASN][1000 genomes]
rs11050966	0.89[ASN][1000 genomes]
rs11050974	1.00[AFR][1000 genomes];0.86[ASN][1000 genomes]
rs11050975	1.00[EUR][1000 genomes];0.86[ASN][1000 genomes]
rs11050976	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];0.86[ASN][1000 genomes]
rs11050978	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];0.86[ASN][1000 genomes]
rs11050979	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];0.86[ASN][1000 genomes]
rs11050980	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];0.86[ASN][1000 genomes]
rs11050982	1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs11050995	1.00[EUR][1000 genomes];0.91[ASN][1000 genomes]
rs11050996	1.00[EUR][1000 genomes];0.83[ASN][1000 genomes]
rs11050997	1.00[EUR][1000 genomes];0.83[ASN][1000 genomes]
rs11050998	1.00[EUR][1000 genomes];0.83[ASN][1000 genomes]
rs11050999	1.00[EUR][1000 genomes];0.83[ASN][1000 genomes]
rs11051000	1.00[EUR][1000 genomes];0.83[ASN][1000 genomes]
rs11051001	1.00[EUR][1000 genomes];0.83[ASN][1000 genomes]
rs11051004	1.00[EUR][1000 genomes];0.83[ASN][1000 genomes]
rs11051011	0.84[EUR][1000 genomes]
rs11051014	0.90[CHB][hapmap];0.90[JPT][hapmap];0.84[EUR][1000 genomes]
rs11051016	0.84[EUR][1000 genomes]
rs11051021	0.84[EUR][1000 genomes]
rs11051024	0.84[EUR][1000 genomes]
rs11051025	0.84[EUR][1000 genomes]
rs11051031	0.90[CHB][hapmap];0.90[JPT][hapmap];0.84[EUR][1000 genomes]
rs11051032	0.90[CHB][hapmap];0.90[JPT][hapmap];0.84[EUR][1000 genomes]
rs11051036	0.90[CHB][hapmap];0.90[JPT][hapmap];0.84[EUR][1000 genomes]
rs11051039	0.90[CHB][hapmap];0.90[JPT][hapmap];0.84[EUR][1000 genomes]
rs11051040	0.90[CHB][hapmap];0.81[JPT][hapmap];0.84[EUR][1000 genomes]
rs11051043	0.84[EUR][1000 genomes]
rs11051064	0.90[CHB][hapmap];0.90[JPT][hapmap];1.00[TSI][hapmap];0.84[EUR][1000 genomes]
rs11051067	0.92[EUR][1000 genomes]
rs11051074	0.92[EUR][1000 genomes]
rs11531057	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];0.92[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs11534760	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs11561156	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs1157125	0.92[EUR][1000 genomes]
rs11613738	0.90[JPT][hapmap]
rs12228212	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];0.83[ASN][1000 genomes]
rs12229358	1.00[EUR][1000 genomes];0.91[ASN][1000 genomes]
rs12229986	0.90[CHB][hapmap];0.84[EUR][1000 genomes]
rs12230006	0.84[EUR][1000 genomes]
rs12230490	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs12231670	0.84[EUR][1000 genomes]
rs16906574	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];0.86[ASN][1000 genomes]
rs16906582	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];0.86[ASN][1000 genomes]
rs16906596	1.00[EUR][1000 genomes];0.83[ASN][1000 genomes]
rs16906601	1.00[EUR][1000 genomes];0.83[ASN][1000 genomes]
rs16906606	1.00[EUR][1000 genomes];0.83[ASN][1000 genomes]
rs16906713	0.84[EUR][1000 genomes]
rs16906758	0.90[CHB][hapmap];0.90[JPT][hapmap];0.84[EUR][1000 genomes]
rs16916147	0.89[CHB][hapmap];0.90[JPT][hapmap];1.00[EUR][1000 genomes];0.83[ASN][1000 genomes]
rs2114900	0.92[EUR][1000 genomes]
rs3850958	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs3889761	1.00[EUR][1000 genomes];0.83[ASN][1000 genomes]
rs3898255	1.00[AMR][1000 genomes];0.92[EUR][1000 genomes]
rs57735299	1.00[EUR][1000 genomes];0.83[ASN][1000 genomes]
rs57918172	0.90[ASN][1000 genomes]
rs60712960	1.00[EUR][1000 genomes];0.83[ASN][1000 genomes]
rs7970293	1.00[EUR][1000 genomes];0.83[ASN][1000 genomes]
rs7977562	0.90[CHB][hapmap];0.90[JPT][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	esv3343291	chr12:30455597-30992837	Weak transcription Enhancers Strong transcription Active TSS Flanking Active TSS Genic enhancers Bivalent/Poised TSS Flanking Bivalent TSS/Enh ZNF genes & repeats Bivalent Enhancer Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	48 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:8 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr12:30739600-30756600	Weak transcription	Pancreas	Pancrea
2	chr12:30748000-30757200	Weak transcription	ES-UCSF4 Cell Line	embryonic stem cell
3	chr12:30752000-30754000	Enhancers	HepG2	liver
4	chr12:30752600-30753800	Enhancers	Fetal Stomach	stomach
5	chr12:30753000-30754400	Enhancers	Fetal Muscle Leg	muscle
6	chr12:30753200-30757400	Weak transcription	Left Ventricle	heart
7	chr12:30753600-30754000	Weak transcription	Esophagus	oesophagus
8	chr12:30753600-30754200	ZNF genes & repeats	Aorta	Aorta

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