Variant report

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

rs_ID	r²[population]
rs10131390	1.00[CEU][hapmap];0.95[AMR][1000 genomes];0.97[EUR][1000 genomes]
rs10135795	0.87[TSI][hapmap];0.81[EUR][1000 genomes]
rs10139602	0.80[EUR][1000 genomes]
rs11159355	0.82[AMR][1000 genomes]
rs11159356	0.91[AMR][1000 genomes];0.92[EUR][1000 genomes]
rs12883984	0.96[CEU][hapmap];0.90[GIH][hapmap];0.83[MEX][hapmap];0.81[TSI][hapmap];0.84[YRI][hapmap];0.89[AMR][1000 genomes];0.89[EUR][1000 genomes]
rs12893958	0.89[CHB][hapmap]
rs2110426	0.81[EUR][1000 genomes]
rs2215837	0.85[TSI][hapmap]
rs60110504	0.85[AMR][1000 genomes];0.84[EUR][1000 genomes]
rs6574440	0.88[TSI][hapmap];0.81[AMR][1000 genomes]
rs6574441	0.88[TSI][hapmap]
rs7149345	0.84[CHB][hapmap];0.80[TSI][hapmap]
rs7157332	0.88[TSI][hapmap]
rs8008554	0.83[CEU][hapmap];0.87[TSI][hapmap];0.81[EUR][1000 genomes]
rs8008709	0.87[TSI][hapmap];0.81[EUR][1000 genomes]
rs8012215	0.85[AMR][1000 genomes];0.82[EUR][1000 genomes];0.83[ASN][1000 genomes]
rs8017044	0.85[TSI][hapmap]
rs8020842	0.87[AMR][1000 genomes];0.90[EUR][1000 genomes]
rs917906	0.96[CEU][hapmap];0.83[TSI][hapmap];0.89[AMR][1000 genomes];0.88[EUR][1000 genomes]
rs965408	0.85[TSI][hapmap]
rs969071	0.87[CEU][hapmap];0.81[CHB][hapmap];0.95[JPT][hapmap]

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	nsv832837	chr14:78766805-78946526	Weak transcription Enhancers Active TSS Flanking Active TSS ZNF genes & repeats Bivalent/Poised TSS Bivalent Enhancer	TF binding region CpG island Chromatin interactive region	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	chr14:78865200-78869400	Weak transcription	Brain Angular Gyrus	brain
2	chr14:78865400-78871200	Weak transcription	Brain Anterior Caudate	brain

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