Variant report

rSNPs within LD-proxies of this variant (count:31)

rs_ID	r²[population]
rs11159406	0.84[EUR][1000 genomes]
rs11844629	0.80[AMR][1000 genomes];0.94[EUR][1000 genomes]
rs11848741	0.92[EUR][1000 genomes]
rs11848812	0.92[EUR][1000 genomes]
rs11848891	0.92[EUR][1000 genomes]
rs11851803	0.92[EUR][1000 genomes]
rs11851933	0.91[EUR][1000 genomes]
rs11851946	0.85[EUR][1000 genomes]
rs12434204	0.87[AFR][1000 genomes]
rs12894028	0.86[AFR][1000 genomes]
rs17110072	0.92[EUR][1000 genomes]
rs17110079	0.80[AMR][1000 genomes];0.94[EUR][1000 genomes]
rs1950447	0.89[AFR][1000 genomes]
rs1950448	0.89[AFR][1000 genomes]
rs1950449	0.89[AFR][1000 genomes];0.95[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs1955878	0.86[AFR][1000 genomes]
rs1955880	0.89[AFR][1000 genomes]
rs1955882	0.89[AFR][1000 genomes]
rs1955885	0.89[AFR][1000 genomes];0.96[ASN][1000 genomes]
rs28599843	0.83[EUR][1000 genomes]
rs55908809	0.80[AMR][1000 genomes];0.94[EUR][1000 genomes]
rs56145536	0.80[AMR][1000 genomes];0.94[EUR][1000 genomes]
rs56756177	0.80[AMR][1000 genomes];0.94[EUR][1000 genomes]
rs6574511	0.81[EUR][1000 genomes]
rs72690495	0.80[AMR][1000 genomes];0.94[EUR][1000 genomes]
rs72692222	0.89[EUR][1000 genomes]
rs72692244	0.85[EUR][1000 genomes]
rs74038014	0.89[EUR][1000 genomes]
rs8011455	0.99[AFR][1000 genomes];0.95[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs8018144	0.89[AFR][1000 genomes]
rs995973	0.88[AFR][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	nsv901519	chr14:25949277-26043929	Weak transcription Enhancers Active TSS Flanking Active TSS	Chromatin interactive region	n/a	inside rSNPs	diseases
2	nsv430993	chr14:25976760-26097160	Active TSS Enhancers ZNF genes & repeats Weak transcription Flanking Active TSS	Chromatin interactive region	n/a	inside rSNPs	diseases

No data

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

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr14:26020800-26025800	Weak transcription	H9 Derived Neuron Cultured Cells	ES cell derived
2	chr14:26022000-26022200	Enhancers	H9 Cell Line	embryonic stem cell

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