chr start stop reference nuc variant nuc depth genic status zygosity variant ID 4 146181600 146181601 T C 46 GENIC homozygous 793698976 4 146181886 146181887 A G 36 GENIC homozygous 793698977 4 146182024 146182025 A G 39 GENIC homozygous 793698978 4 146182137 146182138 G A 36 GENIC homozygous 793698979 4 146184857 146184858 C T 37 GENIC homozygous 793698980 4 146185681 146185682 A C 43 GENIC homozygous 793698981 4 146186320 146186321 T C 35 GENIC homozygous 793698982 4 146188355 146188356 G A 37 GENIC homozygous 793698983 4 146191018 146191019 C T 39 GENIC homozygous 793698984 4 146194601 146194602 T C 32 GENIC homozygous 793698985 4 146196709 146196710 G A 41 GENIC homozygous 793698986