Variant report

rSNPs within LD-proxies of this variant (count:35)

rs_ID	r²[population]
rs10517171	0.83[ASN][1000 genomes]
rs10517172	0.83[ASN][1000 genomes]
rs10517173	0.97[ASN][1000 genomes]
rs10517174	0.83[ASN][1000 genomes]
rs10517175	0.83[ASN][1000 genomes]
rs11727163	1.00[ASN][1000 genomes]
rs11729000	0.86[EUR][1000 genomes]
rs11729961	1.00[AMR][1000 genomes];0.98[EUR][1000 genomes]
rs11731576	0.83[ASN][1000 genomes]
rs11732239	0.80[ASN][1000 genomes]
rs11732398	0.83[ASN][1000 genomes]
rs12512719	0.81[AFR][1000 genomes];1.00[AMR][1000 genomes];0.98[EUR][1000 genomes]
rs16851647	0.83[ASN][1000 genomes]
rs16859823	0.83[ASN][1000 genomes]
rs16859826	0.83[ASN][1000 genomes]
rs16859842	0.86[EUR][1000 genomes]
rs2280072	0.81[ASN][1000 genomes]
rs3762607	0.88[EUR][1000 genomes]
rs3762608	0.88[EUR][1000 genomes]
rs3762610	0.91[EUR][1000 genomes]
rs3762611	0.86[EUR][1000 genomes]
rs3792210	0.92[AMR][1000 genomes];0.91[EUR][1000 genomes]
rs4695182	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];0.98[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs4695183	0.83[ASN][1000 genomes]
rs4695184	0.83[ASN][1000 genomes]
rs57314699	0.83[ASN][1000 genomes]
rs59115556	0.83[ASN][1000 genomes]
rs59481829	0.81[AFR][1000 genomes];1.00[AMR][1000 genomes];0.98[EUR][1000 genomes]
rs59675437	0.83[ASN][1000 genomes]
rs61409453	0.83[ASN][1000 genomes]
rs73813760	0.83[ASN][1000 genomes]
rs73813761	0.83[ASN][1000 genomes]
rs73813771	0.86[EUR][1000 genomes]
rs73813772	0.86[EUR][1000 genomes]
rs73813773	0.86[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	nsv470031	chr4:46982218-47006399	Flanking Bivalent TSS/Enh Active TSS Enhancers Flanking Active TSS Bivalent Enhancer Bivalent/Poised TSS Weak transcription ZNF genes & repeats Transcr. at gene 5' and 3'	TF binding region CpG island	2 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	chr4:46990000-46993400	Weak transcription	Brain Angular Gyrus	brain
2	chr4:46990800-46994000	Enhancers	Fetal Heart	heart
3	chr4:46991200-46993600	Active TSS	Brain Anterior Caudate	brain
4	chr4:46992600-46993400	Weak transcription	Brain Dorsolateral Prefrontal Cortex	brain

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