Variant report

Variant	rs11838990
Chromosome Location	chr13:61371416-61371417
allele	C/T
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 47 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:43)

rs_ID	r²[population]
rs10162120	0.90[AMR][1000 genomes];0.85[EUR][1000 genomes];0.81[ASN][1000 genomes]
rs1028071	0.83[ASN][1000 genomes]
rs1399140	0.97[ASN][1000 genomes]
rs1399141	0.97[ASN][1000 genomes]
rs1399142	0.97[ASN][1000 genomes]
rs1514158	0.97[ASN][1000 genomes]
rs1514168	0.99[ASN][1000 genomes]
rs1855191	0.97[ASN][1000 genomes]
rs1999517	0.96[ASN][1000 genomes]
rs2090087	0.96[ASN][1000 genomes]
rs2184070	0.82[ASN][1000 genomes]
rs2203366	0.97[ASN][1000 genomes]
rs3106554	0.94[ASN][1000 genomes]
rs3106555	0.95[ASN][1000 genomes]
rs3106556	0.83[ASN][1000 genomes]
rs3119864	0.97[ASN][1000 genomes]
rs3119879	0.95[ASN][1000 genomes]
rs3119880	0.83[ASN][1000 genomes]
rs3119882	0.99[ASN][1000 genomes]
rs3119883	0.99[ASN][1000 genomes]
rs3119884	0.99[ASN][1000 genomes]
rs3120232	0.97[ASN][1000 genomes]
rs3127026	0.97[ASN][1000 genomes]
rs3127027	0.83[ASN][1000 genomes]
rs3127029	0.99[ASN][1000 genomes]
rs3127030	0.99[ASN][1000 genomes]
rs3967110	0.92[AMR][1000 genomes];0.90[EUR][1000 genomes];0.83[ASN][1000 genomes]
rs4886268	0.93[AMR][1000 genomes];0.97[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs4886269	0.96[AMR][1000 genomes];0.98[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs4886275	0.97[AFR][1000 genomes];0.99[AMR][1000 genomes];0.98[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs73219646	0.81[AMR][1000 genomes];0.96[EUR][1000 genomes];0.93[ASN][1000 genomes]
rs9285228	0.97[AFR][1000 genomes];0.99[AMR][1000 genomes];0.98[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs9317135	0.80[ASN][1000 genomes]
rs9317136	0.85[AMR][1000 genomes];0.86[EUR][1000 genomes];0.83[ASN][1000 genomes]
rs9317137	0.94[AMR][1000 genomes];0.99[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs9528218	1.00[AFR][1000 genomes];0.99[AMR][1000 genomes];0.98[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs9528220	1.00[AFR][1000 genomes];0.99[AMR][1000 genomes];0.98[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs9538903	0.89[EUR][1000 genomes];0.83[ASN][1000 genomes]
rs9538904	0.92[AMR][1000 genomes];0.85[EUR][1000 genomes];0.82[ASN][1000 genomes]
rs9538922	0.98[AMR][1000 genomes];0.98[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs9538926	0.86[EUR][1000 genomes];0.82[ASN][1000 genomes]
rs9570350	0.82[AMR][1000 genomes]
rs9598169	0.99[ASN][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:4 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv817223	chr13:60623429-61453435	Weak transcription Strong transcription Enhancers Flanking Active TSS Active TSS ZNF genes & repeats Genic enhancers Bivalent/Poised TSS Transcr. at gene 5' and 3' Bivalent Enhancer Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA	41 gene(s)	inside rSNPs	diseases
2	nsv832623	chr13:61303818-61468576	ZNF genes & repeats Enhancers Weak transcription Flanking Active TSS Active TSS	TF binding region CpG island Chromatin interactive region lncRNA	2 gene(s)	inside rSNPs	diseases
3	nsv1037954	chr13:61319533-61395907	Enhancers Weak transcription Flanking Active TSS Active TSS	TF binding region CpG island Chromatin interactive region	2 gene(s)	inside rSNPs	diseases
4	nsv561866	chr13:61328813-61388794	Weak transcription Enhancers Flanking Active TSS Active TSS	TF binding region CpG island Chromatin interactive region	1 gene(s)	inside rSNPs	diseases

No data

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

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr13:61370400-61372000	Weak transcription	Fetal Intestine Small	intestine

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