Variant report

rSNPs within LD-proxies of this variant (count:28)

rs_ID	r²[population]
rs10215057	0.92[EUR][1000 genomes]
rs10215760	0.92[EUR][1000 genomes]
rs10242964	1.00[EUR][1000 genomes]
rs10259832	0.85[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs1364743	1.00[EUR][1000 genomes]
rs1425155	1.00[EUR][1000 genomes]
rs1425163	0.82[EUR][1000 genomes]
rs1425164	0.82[EUR][1000 genomes]
rs1425165	0.82[EUR][1000 genomes]
rs1425166	0.82[EUR][1000 genomes]
rs1593317	0.82[EUR][1000 genomes]
rs1946328	1.00[CEU][hapmap];1.00[CHD][hapmap];1.00[GIH][hapmap];1.00[TSI][hapmap];1.00[EUR][1000 genomes]
rs2349741	0.92[EUR][1000 genomes]
rs2349743	0.85[AMR][1000 genomes];0.92[EUR][1000 genomes]
rs2350167	0.96[EUR][1000 genomes]
rs4584099	0.92[EUR][1000 genomes]
rs4732215	0.92[EUR][1000 genomes]
rs4732216	0.92[EUR][1000 genomes]
rs4732217	0.92[EUR][1000 genomes]
rs6467665	1.00[EUR][1000 genomes]
rs6945197	0.93[AMR][1000 genomes];0.92[EUR][1000 genomes]
rs6946561	1.00[CEU][hapmap]
rs6966702	1.00[EUR][1000 genomes]
rs7796090	0.92[EUR][1000 genomes]
rs9642050	1.00[EUR][1000 genomes]
rs9642054	0.92[EUR][1000 genomes]
rs980193	1.00[EUR][1000 genomes]
rs980194	1.00[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	nsv518439	chr7:136134265-136452082	Enhancers Weak transcription Active TSS ZNF genes & repeats Flanking Active 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	chr7:136175200-136180800	Weak transcription	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
2	chr7:136175400-136179800	Weak transcription	H9 Derived Neuron Cultured Cells	ES cell derived

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