Variant report

Variant	rs72909345
Chromosome Location	chr4:118727448-118727449
allele	A/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 69 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:68)

rs_ID	r²[population]
rs10516640	0.90[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs11098405	0.90[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs11098406	0.90[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs1112975	0.84[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs11562832	0.84[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs11562834	0.86[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs11562842	0.94[EUR][1000 genomes];0.86[ASN][1000 genomes]
rs11562843	0.84[EUR][1000 genomes];0.84[ASN][1000 genomes]
rs11562865	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs11562873	0.94[AFR][1000 genomes];0.97[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs11562874	0.84[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs11562877	0.90[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs11562878	0.88[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs11562900	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs11562902	0.90[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs11562903	0.90[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs11562904	0.90[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs11562920	0.81[AMR][1000 genomes];0.94[EUR][1000 genomes];0.85[ASN][1000 genomes]
rs11930362	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs11934470	0.90[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs11934576	0.90[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs11939447	0.97[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs11939867	0.90[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs17515130	0.94[EUR][1000 genomes];0.85[ASN][1000 genomes]
rs17593478	0.94[EUR][1000 genomes];0.85[ASN][1000 genomes]
rs17862091	0.90[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs17862094	0.90[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs17862099	0.90[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs17862100	0.90[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs17862103	0.81[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs17862104	0.81[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs17862105	0.84[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs17862106	0.86[AFR][1000 genomes];0.97[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs17863010	0.90[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs17863011	0.89[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs17863014	0.90[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs17863020	0.81[AMR][1000 genomes];0.99[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs17863022	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs17863024	0.94[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs17863924	0.90[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs17863937	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs17864925	0.88[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs17866061	0.81[AMR][1000 genomes];0.94[EUR][1000 genomes];0.85[ASN][1000 genomes]
rs17866062	0.95[EUR][1000 genomes];0.86[ASN][1000 genomes]
rs17867559	0.89[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs17867563	0.90[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs17867566	0.81[ASN][1000 genomes]
rs17867567	0.84[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs17867568	0.84[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs17867569	0.84[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs17874660	0.90[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs28512341	1.00[AFR][1000 genomes];0.94[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs28525284	0.97[AMR][1000 genomes];0.85[EUR][1000 genomes];0.93[ASN][1000 genomes]
rs4296744	0.86[EUR][1000 genomes]
rs4580717	0.87[EUR][1000 genomes]
rs55775462	0.87[EUR][1000 genomes]
rs6823636	0.90[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs72909306	0.90[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs72909319	0.84[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs72909324	0.84[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs7661143	0.90[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs7661680	0.90[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs7661688	0.90[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs7670533	0.94[EUR][1000 genomes];0.82[ASN][1000 genomes]
rs7677900	0.90[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs7698673	0.90[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs7699060	0.88[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs7699167	0.90[EUR][1000 genomes];1.00[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	nsv879838	chr4:118681261-118753062	Enhancers Weak transcription Active TSS Bivalent Enhancer Flanking Active TSS	TF binding region CpG island Chromatin interactive region	3 gene(s)	inside rSNPs	diseases

No data

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

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr4:118723200-118728000	Weak transcription	H9 Derived Neuron Cultured Cells	ES cell derived

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