Variant report

Variant	rs4400387
Chromosome Location	chr8:34381462-34381463
allele	A/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 31 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:30)

rs_ID	r²[population]
rs10107624	0.84[AMR][1000 genomes];0.90[ASN][1000 genomes]
rs10111768	0.84[EUR][1000 genomes];0.89[ASN][1000 genomes]
rs12114700	0.87[AMR][1000 genomes];0.90[EUR][1000 genomes];0.87[ASN][1000 genomes]
rs12545278	0.80[ASN][1000 genomes]
rs12547489	0.80[ASN][1000 genomes]
rs1445184	0.99[AFR][1000 genomes];0.95[AMR][1000 genomes];0.85[EUR][1000 genomes];0.94[ASN][1000 genomes]
rs2044355	0.95[AFR][1000 genomes];0.84[AMR][1000 genomes];0.81[ASN][1000 genomes]
rs2166231	0.95[AFR][1000 genomes];0.84[AMR][1000 genomes];0.81[ASN][1000 genomes]
rs28795079	0.88[AMR][1000 genomes];0.85[EUR][1000 genomes];0.87[ASN][1000 genomes]
rs2896967	0.92[AFR][1000 genomes];0.84[AMR][1000 genomes]
rs4144954	0.83[EUR][1000 genomes];0.87[ASN][1000 genomes]
rs4237089	0.82[EUR][1000 genomes];0.81[ASN][1000 genomes]
rs4463416	0.82[EUR][1000 genomes];0.81[ASN][1000 genomes]
rs4534132	0.99[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs4584143	0.84[EUR][1000 genomes];0.89[ASN][1000 genomes]
rs4739580	0.84[AMR][1000 genomes];0.90[ASN][1000 genomes]
rs4739582	0.82[AMR][1000 genomes];0.83[EUR][1000 genomes];0.83[ASN][1000 genomes]
rs4739589	0.81[AMR][1000 genomes];0.89[ASN][1000 genomes]
rs55787309	0.81[AMR][1000 genomes];0.90[ASN][1000 genomes]
rs56406211	0.81[AMR][1000 genomes];0.90[ASN][1000 genomes]
rs6468265	0.99[AFR][1000 genomes];0.95[AMR][1000 genomes];0.84[EUR][1000 genomes];0.93[ASN][1000 genomes]
rs6468266	0.82[ASN][1000 genomes]
rs66516829	0.84[EUR][1000 genomes];0.89[ASN][1000 genomes]
rs66892402	0.99[AFR][1000 genomes];0.95[AMR][1000 genomes];0.87[EUR][1000 genomes];0.94[ASN][1000 genomes]
rs6984972	0.83[EUR][1000 genomes];0.87[ASN][1000 genomes]
rs7833514	0.95[AFR][1000 genomes];0.86[AMR][1000 genomes];0.81[ASN][1000 genomes]
rs7833602	0.88[ASN][1000 genomes]
rs7844647	0.82[AMR][1000 genomes];0.88[EUR][1000 genomes];0.81[ASN][1000 genomes]
rs9297220	0.95[AFR][1000 genomes];0.86[AMR][1000 genomes];0.81[ASN][1000 genomes]
rs953271	0.86[AMR][1000 genomes];0.88[EUR][1000 genomes];0.81[ASN][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	esv3428603	chr8:34367445-34422532	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	chr8:34380600-34381800	Enhancers	Fetal Heart	heart

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