Variant report

Variant	rs10896736
Chromosome Location	chr11:58044783-58044784
allele	G/T
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 100 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:96)

rs_ID	r²[population]
rs10750894	0.98[AFR][1000 genomes];0.97[AMR][1000 genomes];0.98[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs10750895	0.80[EUR][1000 genomes];0.91[ASN][1000 genomes]
rs10750898	0.82[AMR][1000 genomes];0.89[ASN][1000 genomes]
rs10792159	1.00[AFR][1000 genomes];0.94[AMR][1000 genomes];0.98[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs10792165	0.80[EUR][1000 genomes];0.89[ASN][1000 genomes]
rs10896738	1.00[AFR][1000 genomes];0.97[AMR][1000 genomes];0.99[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs10896742	0.81[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs10896748	0.82[ASN][1000 genomes]
rs10896749	0.80[EUR][1000 genomes];0.91[ASN][1000 genomes]
rs10896755	0.80[EUR][1000 genomes];0.89[ASN][1000 genomes]
rs10896760	0.81[AMR][1000 genomes];0.89[ASN][1000 genomes]
rs10896761	0.81[AMR][1000 genomes];0.89[ASN][1000 genomes]
rs10896774	0.87[ASN][1000 genomes]
rs10896775	0.85[ASN][1000 genomes]
rs11229333	1.00[AFR][1000 genomes];0.99[AMR][1000 genomes];0.99[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs11229352	0.82[ASN][1000 genomes]
rs11229353	0.80[EUR][1000 genomes];0.91[ASN][1000 genomes]
rs11229355	0.80[EUR][1000 genomes];0.91[ASN][1000 genomes]
rs11229365	0.80[EUR][1000 genomes];0.91[ASN][1000 genomes]
rs11229366	0.82[AMR][1000 genomes];0.91[ASN][1000 genomes]
rs11229396	0.87[ASN][1000 genomes]
rs11229397	0.87[ASN][1000 genomes]
rs11229423	0.82[ASN][1000 genomes]
rs11607488	0.87[ASN][1000 genomes]
rs12269745	0.87[ASN][1000 genomes]
rs12274866	0.87[ASN][1000 genomes]
rs12278357	0.87[ASN][1000 genomes]
rs12283414	0.87[ASN][1000 genomes]
rs12285111	0.84[ASN][1000 genomes]
rs12286421	0.87[ASN][1000 genomes]
rs12289198	0.87[ASN][1000 genomes]
rs12290089	0.87[ASN][1000 genomes]
rs12291551	0.87[ASN][1000 genomes]
rs12294062	0.82[ASN][1000 genomes]
rs12575804	0.87[ASN][1000 genomes]
rs12786744	0.87[ASN][1000 genomes]
rs12788786	0.87[ASN][1000 genomes]
rs12789701	0.87[ASN][1000 genomes]
rs12797488	0.87[ASN][1000 genomes]
rs12798255	0.87[ASN][1000 genomes]
rs12802819	0.87[ASN][1000 genomes]
rs12802960	0.87[ASN][1000 genomes]
rs12803648	0.87[ASN][1000 genomes]
rs12804134	0.87[ASN][1000 genomes]
rs17474373	0.84[ASN][1000 genomes]
rs1938637	0.81[AMR][1000 genomes];0.89[ASN][1000 genomes]
rs1938646	0.82[AMR][1000 genomes];0.91[ASN][1000 genomes]
rs1938647	0.91[ASN][1000 genomes]
rs1938657	0.80[AMR][1000 genomes];0.91[ASN][1000 genomes]
rs1938658	0.80[AMR][1000 genomes];0.91[ASN][1000 genomes]
rs1938662	0.82[AMR][1000 genomes];0.91[ASN][1000 genomes]
rs1938663	0.80[EUR][1000 genomes];0.91[ASN][1000 genomes]
rs1938664	0.91[ASN][1000 genomes]
rs1986404	0.84[ASN][1000 genomes]
rs2000486	0.91[ASN][1000 genomes]
rs2003231	0.87[ASN][1000 genomes]
rs2186407	0.81[AMR][1000 genomes];0.88[ASN][1000 genomes]
rs2226414	0.89[ASN][1000 genomes]
rs35279927	0.84[ASN][1000 genomes]
rs35542119	0.87[ASN][1000 genomes]
rs3887001	0.80[EUR][1000 genomes];0.91[ASN][1000 genomes]
rs4085405	0.81[AMR][1000 genomes];0.89[ASN][1000 genomes]
rs4127345	0.94[AMR][1000 genomes];0.98[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs4127346	0.91[AFR][1000 genomes];0.96[AMR][1000 genomes];0.98[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs4127348	0.91[ASN][1000 genomes]
rs4127353	0.81[AMR][1000 genomes];0.89[ASN][1000 genomes]
rs4288769	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs4323891	0.81[AMR][1000 genomes];0.89[ASN][1000 genomes]
rs4347409	0.87[ASN][1000 genomes]
rs4439529	1.00[AFR][1000 genomes];0.97[AMR][1000 genomes];0.98[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs4439530	0.90[ASN][1000 genomes]
rs4506677	0.84[ASN][1000 genomes]
rs4517537	0.84[ASN][1000 genomes]
rs4519112	0.86[ASN][1000 genomes]
rs4544018	0.90[ASN][1000 genomes]
rs4561231	0.89[ASN][1000 genomes]
rs4579945	0.84[ASN][1000 genomes]
rs4611223	0.89[ASN][1000 genomes]
rs4611224	0.91[ASN][1000 genomes]
rs4938893	0.82[ASN][1000 genomes]
rs61902844	0.87[ASN][1000 genomes]
rs6591469	0.80[EUR][1000 genomes];0.91[ASN][1000 genomes]
rs6591475	0.84[ASN][1000 genomes]
rs7101864	0.94[AMR][1000 genomes];0.98[EUR][1000 genomes];0.93[ASN][1000 genomes]
rs7102222	0.80[EUR][1000 genomes];0.91[ASN][1000 genomes]
rs7102784	0.94[AMR][1000 genomes];0.98[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs7104814	0.98[AFR][1000 genomes];0.96[AMR][1000 genomes];0.98[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs7110266	0.80[EUR][1000 genomes];0.91[ASN][1000 genomes]
rs7112318	0.81[ASN][1000 genomes]
rs7112578	0.86[ASN][1000 genomes]
rs7117244	0.82[AMR][1000 genomes];0.91[ASN][1000 genomes]
rs7127035	0.80[AFR][1000 genomes];0.97[AMR][1000 genomes];0.98[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs734776	0.81[AMR][1000 genomes];0.89[ASN][1000 genomes]
rs754681	0.82[AMR][1000 genomes];0.89[ASN][1000 genomes]
rs7926741	0.81[AMR][1000 genomes];0.89[ASN][1000 genomes]
rs7931394	0.84[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	nsv1054205	chr11:57544264-58358509	Enhancers Strong transcription Weak transcription Flanking Active TSS Active TSS Genic enhancers ZNF genes & repeats Transcr. at gene 5' and 3' Bivalent/Poised TSS Bivalent Enhancer Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	67 gene(s)	inside rSNPs	diseases
2	nsv897589	chr11:57623815-58052357	Enhancers Weak transcription Flanking Active TSS ZNF genes & repeats Active TSS Strong transcription Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA	24 gene(s)	inside rSNPs	diseases
3	nsv1039453	chr11:57924680-58119650	Enhancers Weak transcription ZNF genes & repeats Flanking Active TSS Active TSS	TF binding region CpG island Chromatin interactive region lncRNA	11 gene(s)	inside rSNPs	diseases
4	nsv541051	chr11:57924680-58119650	Enhancers Weak transcription Flanking Active TSS ZNF genes & repeats Active TSS	TF binding region CpG island Chromatin interactive region lncRNA	11 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:4 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr11:58044000-58044800	Enhancers	NHEK	skin
2	chr11:58044200-58044800	Enhancers	Foreskin Keratinocyte Primary Cells skin03	Skin
3	chr11:58044200-58045000	Enhancers	Foreskin Keratinocyte Primary Cells skin02	Skin
4	chr11:58044600-58059600	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast

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