Variant report

Variant	rs11944084
Chromosome Location	chr4:19569481-19569482
allele	A/G
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:61)

rs_ID	r²[population]
rs10003702	0.89[ASN][1000 genomes]
rs10006103	0.81[ASN][1000 genomes]
rs10006299	0.81[ASN][1000 genomes]
rs10009772	0.84[ASN][1000 genomes]
rs10012861	0.85[ASN][1000 genomes]
rs10025775	0.81[ASN][1000 genomes]
rs10028337	0.84[ASN][1000 genomes]
rs10031579	0.90[ASN][1000 genomes]
rs10032188	0.84[ASN][1000 genomes]
rs10034324	0.81[ASN][1000 genomes]
rs10222803	0.81[ASN][1000 genomes]
rs10222907	0.81[ASN][1000 genomes]
rs10222971	0.81[ASN][1000 genomes]
rs10223045	0.81[ASN][1000 genomes]
rs11933898	0.95[ASN][1000 genomes]
rs11941599	0.85[ASN][1000 genomes]
rs11941815	0.82[ASN][1000 genomes]
rs11945412	0.85[ASN][1000 genomes]
rs11946126	0.82[ASN][1000 genomes]
rs16868608	0.92[ASN][1000 genomes]
rs16868634	0.83[ASN][1000 genomes]
rs28392619	0.81[ASN][1000 genomes]
rs28406392	0.85[ASN][1000 genomes]
rs28505527	0.84[ASN][1000 genomes]
rs28506946	0.82[ASN][1000 genomes]
rs28522472	0.97[AFR][1000 genomes];0.85[ASN][1000 genomes]
rs28625215	0.81[ASN][1000 genomes]
rs28649908	0.85[ASN][1000 genomes]
rs28654609	0.81[ASN][1000 genomes]
rs28662302	0.85[ASN][1000 genomes]
rs28698715	0.81[ASN][1000 genomes]
rs28713269	0.85[ASN][1000 genomes]
rs28749929	0.81[ASN][1000 genomes]
rs28834385	0.81[ASN][1000 genomes]
rs28861473	0.81[ASN][1000 genomes]
rs4380521	0.91[ASN][1000 genomes]
rs4472135	0.91[ASN][1000 genomes]
rs4541506	0.85[ASN][1000 genomes]
rs4572879	0.91[ASN][1000 genomes]
rs4637398	0.85[ASN][1000 genomes]
rs59810064	0.85[ASN][1000 genomes]
rs60069867	0.85[ASN][1000 genomes]
rs60284344	0.92[ASN][1000 genomes]
rs61356602	0.81[ASN][1000 genomes]
rs61359326	0.92[ASN][1000 genomes]
rs62296707	0.85[ASN][1000 genomes]
rs62296709	0.85[ASN][1000 genomes]
rs62299872	0.82[ASN][1000 genomes]
rs62299873	0.81[ASN][1000 genomes]
rs6837423	0.85[ASN][1000 genomes]
rs73097402	0.85[ASN][1000 genomes]
rs73099604	0.85[ASN][1000 genomes]
rs73099613	0.85[ASN][1000 genomes]
rs73099658	0.85[ASN][1000 genomes]
rs73099698	0.92[ASN][1000 genomes]
rs73101116	0.92[ASN][1000 genomes]
rs73101119	0.92[ASN][1000 genomes]
rs9291404	0.91[ASN][1000 genomes]
rs9990468	0.85[ASN][1000 genomes]
rs9994751	0.91[ASN][1000 genomes]
rs9998589	0.82[ASN][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:5 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	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
2	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
3	nsv878734	chr4:19474680-19598710	Enhancers Active TSS Weak transcription Flanking Active TSS ZNF genes & repeats	Chromatin interactive region lncRNA	n/a	inside rSNPs	diseases
4	nsv461286	chr4:19488871-19709795	Enhancers Flanking Active TSS Active TSS Weak transcription ZNF genes & repeats	Chromatin interactive region lncRNA	n/a	inside rSNPs	diseases
5	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	chr4:19569400-19570200	Weak transcription	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
2	chr4:19569400-19571000	Enhancers	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived

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