Table 3. Genes located in the genomic regions for the significant single-nucleotide polymorphisms

Trait	Chr	Start position (bp)	End position (bp)	Genes
Arginine, Inosine	1	170,065,610	170,700,171	RB1, LPAR6, RCBTB2, CYSLTR2, FNDC3A, MLNR, CDADC1, CAB39L, SETDB2, PHF11, RCBTB1, ARL11, KPNA3, SPRYD7, TRIM13, KCNRG
Arginine, Essential FAAs	2	32,588,887	33,940,447	HOXA3, HOXA4, HOXA5, HOXA6, HOXA7, HOXA9, HOXA10, HOXA11, HOXA13, EVX1, HIBADH, TAX1BP1, JAZF1, CREB5, TRIL, CHN2, WIPF3, SCRN1, FKBP14, PLEKHA8
Arginine, Essential FAAs	7	30,761,616	31,457,806	CXCR4, THSD7B, HNMT, SPOPL, NXPH2
Inosine	4	74,767,885	75,920,712	KCNIP4, ADGRA3, PPARGC1A, LDB2, QDPR, CLRN2, LAP3, MED28, FAM184B, LCORL, NCAPG
Glycine	1	81,317,906	82,292,366	CHD1L, FAAHL, TMEM39A, B4GALT4, B4GALTL, B3GAT1L, UPK1B, IGSF11, LSAMP
Threonine	3	108,221,189	108,846,159	TFAP2B, TFAP2D, CRISP3, CRISP2, RHAG, CYP2AC1, CYP2AC2, CENPQ, MMUT, OPN5L2, CDC5L

Chr, chromosome; bp, base pair; FAA, free amino acid.