chr start stop reference nuc variant nuc depth genic status zygosity variant ID 1 263812471 263812472 G A 26 GENIC homozygous 948973809 1 263813164 263813165 C A 20 GENIC homozygous 948973810 1 263813314 263813315 G A 24 GENIC homozygous 948973811 1 263813492 263813493 T A 11 GENIC homozygous 948973812 1 263814051 263814052 C T 24 GENIC homozygous 948973813 1 263815744 263815745 A G 25 GENIC homozygous 948973814 1 263817743 263817744 A G 12 GENIC homozygous 948973815 1 263820813 263820814 A G 23 GENIC homozygous 948973816 1 263820861 263820862 C T 19 GENIC homozygous 948973817 1 263821401 263821402 G A 26 GENIC homozygous 948973818 1 263823231 263823232 G A 15 GENIC homozygous 948973819 1 263823243 263823244 C T 16 GENIC homozygous 948973820 1 263823512 263823513 A G 21 GENIC homozygous 948973821 1 263825765 263825766 G T 13 GENIC homozygous 948973822 1 263827331 263827332 G A 17 GENIC homozygous 948973823 1 263828502 263828503 C A 11 GENIC possibly homozygous 948973824 1 263831722 263831723 C T 26 GENIC homozygous 948973825 1 263832115 263832116 T C 21 GENIC homozygous 948973826 1 263832813 263832814 A G 21 GENIC homozygous 948973827 1 263835278 263835279 C T 23 GENIC homozygous 948973828 1 263835926 263835927 G A 21 GENIC homozygous 948973829 1 263837493 263837494 G A 19 GENIC homozygous 948973830 1 263840846 263840847 C T 21 GENIC homozygous 948973831 1 263842282 263842283 G T 18 GENIC homozygous 948973832 1 263843300 263843301 A T 23 GENIC homozygous 948973833 1 263844963 263844964 A G 21 GENIC homozygous 948973834