Variant report

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

rs_ID	r²[population]
rs12573890	0.86[AMR][1000 genomes];0.87[EUR][1000 genomes]
rs12573976	0.80[EUR][1000 genomes]
rs12575408	0.87[EUR][1000 genomes]
rs12576286	0.80[EUR][1000 genomes]
rs12576891	0.83[AMR][1000 genomes];0.87[EUR][1000 genomes]
rs12577107	0.90[AMR][1000 genomes];1.00[EUR][1000 genomes];0.92[ASN][1000 genomes]
rs12577528	0.87[EUR][1000 genomes]
rs1455100	0.87[EUR][1000 genomes]
rs1455101	0.87[EUR][1000 genomes]
rs16924862	0.80[EUR][1000 genomes]
rs16932620	0.87[EUR][1000 genomes]
rs16932622	0.80[EUR][1000 genomes]
rs16932625	0.87[EUR][1000 genomes]
rs16932630	0.87[EUR][1000 genomes]
rs16932634	0.84[AMR][1000 genomes];0.87[EUR][1000 genomes]
rs16932650	0.80[EUR][1000 genomes]
rs16932653	0.80[EUR][1000 genomes]
rs16932655	0.80[EUR][1000 genomes]
rs16932664	0.80[EUR][1000 genomes]
rs16932670	0.80[EUR][1000 genomes]
rs1840422	0.80[EUR][1000 genomes]
rs35972839	0.87[EUR][1000 genomes]
rs55689121	0.87[EUR][1000 genomes]
rs55865094	0.87[EUR][1000 genomes]
rs55882244	0.87[EUR][1000 genomes]
rs59412323	0.87[EUR][1000 genomes]
rs61094171	0.88[AMR][1000 genomes];0.87[EUR][1000 genomes]
rs61347512	0.84[AMR][1000 genomes];0.87[EUR][1000 genomes]
rs7110987	0.80[EUR][1000 genomes]
rs7126432	0.80[EUR][1000 genomes]
rs7932204	0.80[EUR][1000 genomes]
rs7935396	0.87[EUR][1000 genomes]
rs7936647	0.80[EUR][1000 genomes]
rs966933	0.87[EUR][1000 genomes]
rs993698	0.87[EUR][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	nsv553562	chr11:16112180-16220289	Enhancers Weak transcription Strong transcription Flanking Active TSS Active TSS ZNF genes & repeats Bivalent/Poised TSS Genic enhancers Bivalent Enhancer	TF binding region CpG island Chromatin interactive region	2 gene(s)	inside rSNPs	diseases
2	nsv529731	chr11:16122782-16468170	Enhancers Active TSS Bivalent Enhancer Weak transcription Flanking Active TSS ZNF genes & repeats Strong transcription Genic enhancers Flanking Bivalent TSS/Enh Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA	2 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:2 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr11:16158400-16169200	Weak transcription	Ganglion Eminence derived primary cultured neurospheres	brain
2	chr11:16163400-16170000	Weak transcription	ES-UCSF4 Cell Line	embryonic stem cell

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