Variant report

Variant	rs67047416
Chromosome Location	chr3:88078627-88078628
allele	A/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 55 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:53)

rs_ID	r²[population]
rs10511136	0.84[AMR][1000 genomes];0.97[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs11128018	0.92[AFR][1000 genomes];0.97[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs11128019	0.90[AFR][1000 genomes];0.97[AMR][1000 genomes];0.99[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs11717413	0.87[AMR][1000 genomes];0.97[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs11915058	0.92[AFR][1000 genomes];0.97[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs12714696	0.84[EUR][1000 genomes]
rs13074576	0.84[EUR][1000 genomes]
rs1431153	0.81[AMR][1000 genomes];0.87[EUR][1000 genomes]
rs1469569	0.87[AMR][1000 genomes];0.95[EUR][1000 genomes];0.82[ASN][1000 genomes]
rs1503433	0.84[EUR][1000 genomes]
rs1604699	0.84[EUR][1000 genomes]
rs17549213	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];0.99[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs17549345	0.97[AFR][1000 genomes];0.97[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs1835542	0.81[AMR][1000 genomes];0.87[EUR][1000 genomes]
rs1835543	0.83[EUR][1000 genomes]
rs2016224	0.84[EUR][1000 genomes]
rs2099229	0.84[EUR][1000 genomes]
rs2163423	0.83[AMR][1000 genomes];0.88[EUR][1000 genomes]
rs2344185	0.84[AMR][1000 genomes];0.91[EUR][1000 genomes];0.92[ASN][1000 genomes]
rs2880801	0.84[EUR][1000 genomes]
rs2880802	0.84[EUR][1000 genomes]
rs35040143	0.81[AMR][1000 genomes];0.87[EUR][1000 genomes]
rs4858925	0.84[EUR][1000 genomes]
rs4858969	0.84[EUR][1000 genomes]
rs4858971	0.83[EUR][1000 genomes]
rs4858972	0.83[EUR][1000 genomes]
rs4858974	0.81[AMR][1000 genomes];0.87[EUR][1000 genomes]
rs4858975	0.81[AMR][1000 genomes];0.87[EUR][1000 genomes]
rs55644022	0.81[ASN][1000 genomes]
rs55840331	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];0.99[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs56006017	0.86[ASN][1000 genomes]
rs56173847	0.88[ASN][1000 genomes]
rs60099577	0.97[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs6551264	0.81[ASN][1000 genomes]
rs6770013	0.83[EUR][1000 genomes]
rs6778211	0.84[EUR][1000 genomes]
rs6781226	0.84[EUR][1000 genomes]
rs6781901	0.81[AMR][1000 genomes];0.87[EUR][1000 genomes]
rs6785333	0.84[AMR][1000 genomes];0.94[EUR][1000 genomes];0.95[ASN][1000 genomes]
rs68042814	0.97[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs73144053	0.82[ASN][1000 genomes]
rs7629565	0.84[EUR][1000 genomes]
rs7630716	0.84[EUR][1000 genomes]
rs7637503	0.87[AMR][1000 genomes];0.96[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs7652406	0.84[EUR][1000 genomes]
rs9310061	0.81[AMR][1000 genomes];0.87[EUR][1000 genomes]
rs9852704	0.84[AMR][1000 genomes];0.91[EUR][1000 genomes];0.92[ASN][1000 genomes]
rs9855839	0.84[EUR][1000 genomes]
rs9859034	0.84[AMR][1000 genomes];0.91[EUR][1000 genomes];0.92[ASN][1000 genomes]
rs9861809	0.84[EUR][1000 genomes]
rs9863076	0.84[EUR][1000 genomes]
rs9878862	0.84[EUR][1000 genomes]
rs9880480	0.84[AMR][1000 genomes];0.91[EUR][1000 genomes];0.92[ASN][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:2 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv877146	chr3:87983962-88159835	Weak transcription ZNF genes & repeats Enhancers Active TSS Flanking Active TSS Genic enhancers Strong transcription Transcr. at gene 5' and 3' Bivalent/Poised TSS Bivalent Enhancer Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region	12 gene(s)	inside rSNPs	diseases
2	nsv536635	chr3:88049304-88088520	Flanking Active TSS Weak transcription Active TSS Enhancers Bivalent Enhancer Flanking Bivalent TSS/Enh Bivalent/Poised TSS ZNF genes & repeats	Chromatin interactive region	2 gene(s)	inside rSNPs	n/a

No data

Chromatin state (count:4 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr3:88073600-88080600	Weak transcription	Thymus	Thymus
2	chr3:88078200-88080800	Weak transcription	Left Ventricle	heart
3	chr3:88078600-88079200	Enhancers	Primary T helper memory cells from peripheral blood 1	blood
4	chr3:88078600-88079400	Enhancers	Primary T killer memory cells from peripheral blood	blood

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