Table 1.

Known ZEB2-associated GWAS SNPs that are related to the risk of CAD.

SNP ID	Location on chromosome 2	Reference allele	CAD risk allele	Allele frequency	Gene name	Function	Nearby gene(s)	Beta of risk allele	GWAS p value*	References
rs2252641	145043894	T	C	T=0.307; C=0.693	TEX41	intron	LINC01966, AC096666.1	−0.0368	5.00× 10−13	(6, 7, 14, 15)
rs1830321	145067988	C	T	C=0.503; T=0.497	TEX41	intron	LINC01966, AC096666.1	0.033	3.19×10−8	(6, 9)
rs6740731	144513025	G	A/C/T	G=0.679; A=0.321	ZEB2	intron or 3’UTR	ZEB2-AS1	0.0457	2.77×10−9	(6, 14, 15)
rs17678683	144528992	T	G	T=0.938; G=0.062	LINC01412	intron	ZEB2, ZEB2-AS1	−0.0988	3.00×10−9	(6, 7, 12, 14, 15)

^*The lowest p value is provided from across all the cited CAD GWAS studies, respectively. See also Figure 1.