Variant report

Variant	rs73834808
Chromosome Location	chr3:68113859-68113860
allele	C/T
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:47)

rs_ID	r²[population]
rs1351957	0.86[AMR][1000 genomes]
rs17140939	0.86[AMR][1000 genomes]
rs17140941	0.86[AMR][1000 genomes]
rs17140947	0.86[AMR][1000 genomes];0.90[EUR][1000 genomes]
rs17140948	0.86[AMR][1000 genomes];0.90[EUR][1000 genomes]
rs55780642	0.84[AFR][1000 genomes];0.93[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs57457619	0.86[AMR][1000 genomes];0.93[ASN][1000 genomes]
rs58063220	0.86[AMR][1000 genomes];0.90[EUR][1000 genomes]
rs59728287	0.81[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs60547129	0.87[AFR][1000 genomes];0.93[AMR][1000 genomes];1.00[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs61737909	0.86[AMR][1000 genomes];0.86[ASN][1000 genomes]
rs61739210	0.86[AMR][1000 genomes];0.85[ASN][1000 genomes]
rs72626932	0.86[AMR][1000 genomes]
rs73834809	1.00[AFR][1000 genomes];0.93[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs73834814	0.86[AMR][1000 genomes];0.90[EUR][1000 genomes]
rs73834815	0.95[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs73834816	0.87[AFR][1000 genomes];0.93[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs73834820	0.86[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs73834821	0.90[EUR][1000 genomes]
rs73834822	0.86[AMR][1000 genomes];0.90[EUR][1000 genomes]
rs73834823	0.86[AMR][1000 genomes];0.90[EUR][1000 genomes]
rs73834824	0.81[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs73834825	0.93[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs73834826	0.86[AMR][1000 genomes];0.90[EUR][1000 genomes]
rs73834828	0.86[AMR][1000 genomes];0.85[EUR][1000 genomes];0.95[ASN][1000 genomes]
rs73834833	0.86[AMR][1000 genomes]
rs73834835	0.86[AMR][1000 genomes];0.93[ASN][1000 genomes]
rs73834837	0.86[AMR][1000 genomes];0.93[ASN][1000 genomes]
rs73834838	0.86[AMR][1000 genomes]
rs73834839	0.86[AMR][1000 genomes];0.93[ASN][1000 genomes]
rs73834844	0.86[AMR][1000 genomes];0.93[ASN][1000 genomes]
rs73834845	0.86[AMR][1000 genomes];0.93[ASN][1000 genomes]
rs73834846	0.86[AMR][1000 genomes];0.93[ASN][1000 genomes]
rs73834847	0.86[AMR][1000 genomes]
rs73834852	0.86[AMR][1000 genomes];0.90[ASN][1000 genomes]
rs73837231	0.86[AMR][1000 genomes];0.90[EUR][1000 genomes]
rs73837233	0.86[AMR][1000 genomes];0.90[EUR][1000 genomes]
rs73837236	0.86[AMR][1000 genomes];0.90[EUR][1000 genomes]
rs73837237	0.86[AMR][1000 genomes];0.90[EUR][1000 genomes]
rs73837249	0.86[AMR][1000 genomes];0.90[EUR][1000 genomes]
rs73837250	0.86[AMR][1000 genomes];0.90[EUR][1000 genomes]
rs73837251	0.86[AMR][1000 genomes];0.90[EUR][1000 genomes]
rs73837263	0.86[AMR][1000 genomes];1.00[EUR][1000 genomes];0.89[ASN][1000 genomes]
rs73837269	0.86[AMR][1000 genomes];1.00[EUR][1000 genomes];0.95[ASN][1000 genomes]
rs73837270	0.86[AMR][1000 genomes];0.90[EUR][1000 genomes]
rs7426725	0.95[AFR][1000 genomes];0.86[AMR][1000 genomes];0.95[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs7433199	0.95[AFR][1000 genomes];0.93[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:8 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv1002010	chr3:67785913-68312064	Enhancers Flanking Active TSS Weak transcription Active TSS Flanking Bivalent TSS/Enh Bivalent/Poised TSS ZNF genes & repeats Bivalent Enhancer Strong transcription	TF binding region CpG island Chromatin interactive region lncRNA	9 gene(s)	inside rSNPs	diseases
2	nsv1009871	chr3:67862617-68312064	Flanking Active TSS Enhancers Weak transcription Active TSS Bivalent/Poised TSS Flanking Bivalent TSS/Enh Bivalent Enhancer ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA	7 gene(s)	inside rSNPs	diseases
3	nsv536583	chr3:67862617-68312064	Active TSS Enhancers Weak transcription Flanking Active TSS Bivalent/Poised TSS Flanking Bivalent TSS/Enh Bivalent Enhancer ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA	7 gene(s)	inside rSNPs	diseases
4	nsv1010231	chr3:67894825-68117879	Flanking Active TSS Enhancers Bivalent Enhancer Weak transcription Bivalent/Poised TSS Active TSS Flanking Bivalent TSS/Enh ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA	4 gene(s)	inside rSNPs	diseases
5	nsv999747	chr3:68066423-68188180	Enhancers Weak transcription Flanking Active TSS Active TSS ZNF genes & repeats	Chromatin interactive region	n/a	inside rSNPs	diseases
6	nsv536584	chr3:68066423-68188180	Enhancers Flanking Active TSS Weak transcription ZNF genes & repeats Active TSS	Chromatin interactive region	n/a	inside rSNPs	diseases
7	esv2752014	chr3:68091879-68416989	Enhancers Weak transcription Active TSS ZNF genes & repeats Flanking Active TSS	TF binding region CpG island Chromatin interactive region	4 gene(s)	inside rSNPs	diseases
8	nsv1007450	chr3:68094416-68346546	Enhancers Weak transcription ZNF genes & repeats Flanking Active TSS Active TSS	TF binding region CpG island Chromatin interactive region	3 gene(s)	inside rSNPs	diseases

No data

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

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr3:68110800-68124000	Weak transcription	Primary T helper naive cells from peripheral blood	blood
2	chr3:68111600-68119800	Weak transcription	Primary T helper memory cells from peripheral blood 1	blood
3	chr3:68112800-68114400	Enhancers	Fetal Brain Male	brain
4	chr3:68113400-68114000	Enhancers	Cortex derived primary cultured neurospheres	brain

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