Variant report

Variant	rs2719298
Chromosome Location	chr8:34263605-34263606
allele	A/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 68 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:67)

rs_ID	r²[population]
rs10089816	0.84[EUR][1000 genomes]
rs10100684	0.84[EUR][1000 genomes]
rs10101147	0.85[EUR][1000 genomes]
rs10110278	0.90[EUR][1000 genomes]
rs10112924	0.86[EUR][1000 genomes]
rs1014493	0.87[EUR][1000 genomes]
rs10447956	0.86[EUR][1000 genomes]
rs11990673	0.85[EUR][1000 genomes]
rs12541738	0.86[EUR][1000 genomes]
rs13264902	0.82[EUR][1000 genomes]
rs13272790	0.81[EUR][1000 genomes]
rs13277369	0.86[EUR][1000 genomes]
rs13280754	0.85[EUR][1000 genomes]
rs1348639	0.83[AMR][1000 genomes];1.00[ASN][1000 genomes]
rs1348640	0.90[EUR][1000 genomes]
rs1350558	0.80[ASN][1000 genomes]
rs1373803	0.89[AMR][1000 genomes];0.93[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs1445182	0.87[EUR][1000 genomes]
rs1445183	0.87[EUR][1000 genomes]
rs1445199	0.80[EUR][1000 genomes];0.84[ASN][1000 genomes]
rs1458909	0.96[AFR][1000 genomes];0.94[EUR][1000 genomes];0.87[ASN][1000 genomes]
rs1458910	0.87[EUR][1000 genomes]
rs1458913	0.81[ASN][1000 genomes]
rs1458914	0.81[ASN][1000 genomes]
rs1463510	0.83[ASN][1000 genomes]
rs1562182	0.87[EUR][1000 genomes]
rs1978999	0.86[EUR][1000 genomes]
rs1979298	0.86[EUR][1000 genomes]
rs2028773	0.80[EUR][1000 genomes];0.84[ASN][1000 genomes]
rs2120917	0.87[EUR][1000 genomes]
rs2120919	0.86[EUR][1000 genomes]
rs2590455	0.87[EUR][1000 genomes]
rs2590456	0.81[EUR][1000 genomes]
rs2590457	0.87[EUR][1000 genomes]
rs2590459	0.87[EUR][1000 genomes]
rs2590460	0.87[EUR][1000 genomes]
rs2609592	0.90[AMR][1000 genomes];0.93[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs2609604	0.87[EUR][1000 genomes]
rs2609605	0.87[EUR][1000 genomes]
rs2609613	0.87[EUR][1000 genomes]
rs2609634	0.82[ASN][1000 genomes]
rs2719270	0.81[EUR][1000 genomes];0.84[ASN][1000 genomes]
rs2719287	0.86[EUR][1000 genomes]
rs2719306	0.83[ASN][1000 genomes]
rs2719317	0.87[EUR][1000 genomes]
rs2719319	0.81[ASN][1000 genomes]
rs2719324	0.81[ASN][1000 genomes]
rs28521494	0.82[EUR][1000 genomes]
rs4308727	0.87[EUR][1000 genomes]
rs4322005	0.85[EUR][1000 genomes]
rs4475478	0.87[EUR][1000 genomes]
rs4475479	0.85[EUR][1000 genomes]
rs4739566	0.83[EUR][1000 genomes]
rs6468255	0.85[EUR][1000 genomes]
rs6468256	0.83[EUR][1000 genomes]
rs6468257	0.80[EUR][1000 genomes]
rs6985772	0.86[EUR][1000 genomes]
rs6986938	0.86[EUR][1000 genomes]
rs6988429	0.85[EUR][1000 genomes]
rs6988737	0.84[EUR][1000 genomes]
rs7011041	0.88[EUR][1000 genomes]
rs7812560	0.85[EUR][1000 genomes]
rs7822096	0.84[EUR][1000 genomes]
rs7841483	0.82[EUR][1000 genomes]
rs7842180	0.85[EUR][1000 genomes]
rs7843364	0.85[EUR][1000 genomes]
rs958085	0.87[EUR][1000 genomes]

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	esv3358387	chr8:34262310-34265908	Enhancers Weak transcription	Chromatin interactive region	n/a	inside rSNPs	diseases

No data

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

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr8:34261200-34269800	Weak transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived

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