Variant report

rSNPs within LD-proxies of this variant (count:24)

rs_ID	r²[population]
rs10048650	0.81[AFR][1000 genomes];0.84[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs1362487	0.85[AFR][1000 genomes]
rs1362493	0.81[AMR][1000 genomes]
rs1362494	0.81[AMR][1000 genomes]
rs1362496	1.00[EUR][1000 genomes]
rs1420387	0.89[AFR][1000 genomes]
rs1420389	0.84[AFR][1000 genomes];0.92[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs1548903	1.00[EUR][1000 genomes]
rs2192987	0.84[AMR][1000 genomes]
rs2287110	0.82[AFR][1000 genomes]
rs2287111	0.82[AFR][1000 genomes]
rs2883886	0.92[AFR][1000 genomes]
rs2883887	0.81[AFR][1000 genomes];0.84[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs34856125	1.00[EUR][1000 genomes]
rs45617531	1.00[EUR][1000 genomes]
rs4668317	0.85[AFR][1000 genomes]
rs4668321	0.87[AFR][1000 genomes]
rs4668323	0.84[AMR][1000 genomes]
rs6721280	0.81[AFR][1000 genomes];1.00[EUR][1000 genomes]
rs6733154	0.81[AFR][1000 genomes];0.92[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs6749003	0.81[AFR][1000 genomes];0.84[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs6750787	0.84[AMR][1000 genomes]
rs73023326	1.00[EUR][1000 genomes]
rs7597182	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	esv1806894	chr2:171651783-171679041	Bivalent/Poised TSS Flanking Bivalent TSS/Enh Bivalent Enhancer Enhancers Active TSS Weak transcription Flanking Active TSS Transcr. at gene 5' and 3' Strong transcription	TF binding region CpG island Chromatin interactive region lncRNA	6 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	chr2:171629600-171658800	Weak transcription	Ganglion Eminence derived primary cultured neurospheres	brain
2	chr2:171642400-171669000	Weak transcription	Cortex derived primary cultured neurospheres	brain

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