Variant report

rSNPs within LD-proxies of this variant (count:22)

rs_ID	r²[population]
rs10219211	1.00[ASN][1000 genomes]
rs10502256	1.00[ASN][1000 genomes]
rs11218409	0.95[ASN][1000 genomes]
rs11218414	0.94[ASN][1000 genomes]
rs11218415	0.94[ASN][1000 genomes]
rs11218416	0.94[ASN][1000 genomes]
rs11218435	0.94[ASN][1000 genomes]
rs11218439	0.94[ASN][1000 genomes]
rs12273557	0.94[ASN][1000 genomes]
rs12276466	0.95[ASN][1000 genomes]
rs12277681	1.00[ASN][1000 genomes]
rs12277948	1.00[ASN][1000 genomes]
rs12282527	1.00[ASN][1000 genomes]
rs12287945	0.94[ASN][1000 genomes]
rs12290988	1.00[ASN][1000 genomes]
rs1789763	0.82[AFR][1000 genomes];0.92[AMR][1000 genomes];0.95[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs28378150	0.94[ASN][1000 genomes]
rs61903403	0.94[ASN][1000 genomes]
rs7935547	0.94[ASN][1000 genomes]
rs7938656	0.94[ASN][1000 genomes]
rs7940956	1.00[ASN][1000 genomes]
rs7941972	0.94[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	nsv832287	chr11:121575379-121722735	Weak transcription Flanking Active TSS Enhancers Bivalent Enhancer Active TSS ZNF genes & repeats Flanking Bivalent TSS/Enh Bivalent/Poised TSS	Chromatin interactive region	2 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:3 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr11:121714800-121715600	Enhancers	Brain Anterior Caudate	brain
2	chr11:121714800-121715800	Enhancers	Brain Inferior Temporal Lobe	brain
3	chr11:121715200-121715800	Enhancers	Brain Substantia Nigra	brain

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