Variant report

Variant	rs11941599
Chromosome Location	chr4:19496837-19496838
allele	G/T
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 92 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:86)

rs_ID	r²[population]
rs10003702	0.89[ASN][1000 genomes]
rs10006103	0.96[ASN][1000 genomes]
rs10006299	0.96[ASN][1000 genomes]
rs10009772	0.99[ASN][1000 genomes]
rs10012861	1.00[ASN][1000 genomes]
rs10015294	0.92[ASN][1000 genomes]
rs10025775	0.96[ASN][1000 genomes]
rs10028337	0.99[ASN][1000 genomes]
rs10031579	0.89[ASN][1000 genomes]
rs10032188	0.99[ASN][1000 genomes]
rs10032629	0.92[ASN][1000 genomes]
rs10034324	0.96[ASN][1000 genomes]
rs10212992	0.88[ASN][1000 genomes]
rs10222803	0.96[ASN][1000 genomes]
rs10222907	0.96[ASN][1000 genomes]
rs10222971	0.95[ASN][1000 genomes]
rs10223045	0.96[ASN][1000 genomes]
rs10470799	0.90[ASN][1000 genomes]
rs11933898	0.89[ASN][1000 genomes]
rs11941815	0.97[ASN][1000 genomes]
rs11943058	0.86[ASN][1000 genomes]
rs11943773	0.86[ASN][1000 genomes]
rs11944084	0.85[ASN][1000 genomes]
rs11945412	0.98[AFR][1000 genomes];0.94[AMR][1000 genomes];0.99[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs11946126	0.97[ASN][1000 genomes]
rs13434929	0.87[ASN][1000 genomes]
rs1388145	0.87[ASN][1000 genomes]
rs1388148	0.90[ASN][1000 genomes]
rs16868608	0.92[ASN][1000 genomes]
rs16868634	0.82[ASN][1000 genomes]
rs28392619	0.96[ASN][1000 genomes]
rs28406392	1.00[ASN][1000 genomes]
rs28445313	0.89[ASN][1000 genomes]
rs28468581	0.92[ASN][1000 genomes]
rs28505527	0.99[ASN][1000 genomes]
rs28506946	0.97[ASN][1000 genomes]
rs28584356	0.90[ASN][1000 genomes]
rs28612466	0.89[ASN][1000 genomes]
rs28625215	0.96[ASN][1000 genomes]
rs28649908	1.00[ASN][1000 genomes]
rs28654609	0.96[ASN][1000 genomes]
rs28662302	0.96[AFR][1000 genomes];0.94[AMR][1000 genomes];0.97[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs28675174	0.92[ASN][1000 genomes]
rs28698715	0.96[ASN][1000 genomes]
rs28713269	1.00[ASN][1000 genomes]
rs28749929	0.96[ASN][1000 genomes]
rs28809022	0.92[ASN][1000 genomes]
rs28834385	0.96[ASN][1000 genomes]
rs28849735	0.92[ASN][1000 genomes]
rs28861473	0.96[ASN][1000 genomes]
rs4380521	0.90[ASN][1000 genomes]
rs4472135	0.90[ASN][1000 genomes]
rs4541506	0.98[AFR][1000 genomes];1.00[AMR][1000 genomes];0.98[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs4572879	0.90[ASN][1000 genomes]
rs4637398	0.98[AFR][1000 genomes];1.00[AMR][1000 genomes];0.98[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs59192349	0.87[ASN][1000 genomes]
rs59810064	1.00[ASN][1000 genomes]
rs60069867	1.00[ASN][1000 genomes]
rs60284344	0.92[ASN][1000 genomes]
rs61359326	0.92[ASN][1000 genomes]
rs62296707	1.00[ASN][1000 genomes]
rs62296709	1.00[ASN][1000 genomes]
rs62298737	0.92[ASN][1000 genomes]
rs62299872	0.81[ASN][1000 genomes]
rs6837423	0.96[AFR][1000 genomes];0.93[AMR][1000 genomes];0.97[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs73092965	0.92[ASN][1000 genomes]
rs73092970	0.92[ASN][1000 genomes]
rs73092977	0.92[ASN][1000 genomes]
rs73092981	0.92[ASN][1000 genomes]
rs73092983	0.92[ASN][1000 genomes]
rs73092984	0.92[ASN][1000 genomes]
rs73097402	1.00[ASN][1000 genomes]
rs73099604	1.00[ASN][1000 genomes]
rs73099613	1.00[ASN][1000 genomes]
rs73099658	1.00[ASN][1000 genomes]
rs73099698	0.92[ASN][1000 genomes]
rs73101116	0.92[ASN][1000 genomes]
rs73101119	0.92[ASN][1000 genomes]
rs73110735	0.90[ASN][1000 genomes]
rs73110746	0.87[ASN][1000 genomes]
rs9291404	0.90[ASN][1000 genomes]
rs982066	0.90[ASN][1000 genomes]
rs982067	0.90[ASN][1000 genomes]
rs9990468	1.00[ASN][1000 genomes]
rs9994751	0.90[ASN][1000 genomes]
rs9998589	0.97[ASN][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:6 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv593785	chr4:19092157-19521956	Enhancers Weak transcription Flanking Active TSS Bivalent Enhancer ZNF genes & repeats Active TSS	TF binding region CpG island Chromatin interactive region lncRNA	3 gene(s)	inside rSNPs	diseases
2	nsv878732	chr4:19172031-19660947	Enhancers Weak transcription Flanking Active TSS ZNF genes & repeats Active TSS Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA	3 gene(s)	inside rSNPs	diseases
3	nsv878733	chr4:19335464-19928602	Enhancers Weak transcription Flanking Active TSS Active TSS ZNF genes & repeats Bivalent Enhancer Genic enhancers	TF binding region CpG island Chromatin interactive region lncRNA	6 gene(s)	inside rSNPs	diseases
4	nsv878734	chr4:19474680-19598710	Enhancers Active TSS Weak transcription Flanking Active TSS ZNF genes & repeats	Chromatin interactive region lncRNA	n/a	inside rSNPs	diseases
5	nsv461286	chr4:19488871-19709795	Enhancers Flanking Active TSS Active TSS Weak transcription ZNF genes & repeats	Chromatin interactive region lncRNA	n/a	inside rSNPs	diseases
6	nsv593786	chr4:19488871-19709795	Enhancers Weak transcription ZNF genes & repeats Active TSS Flanking Active TSS	Chromatin interactive region lncRNA	n/a	inside rSNPs	diseases

No data

Chromatin state (count:2 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr4:19496000-19497000	Enhancers	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
2	chr4:19496800-19497400	Enhancers	Muscle Satellite Cultured Cells	--

The 2.0 version of rSNPBase

Variant report

Quick Search:

what's new

Quick links