chr start stop reference nuc variant nuc depth genic status zygosity variant ID 1 263812471 263812472 G A 58 GENIC homozygous 806123905 1 263813164 263813165 C A 54 GENIC possibly homozygous 806123906 1 263813492 263813493 T A 51 GENIC homozygous 806123907 1 263814011 263814012 C T 41 GENIC homozygous 806123908 1 263814051 263814052 C T 53 GENIC possibly homozygous 806123909 1 263814338 263814339 G A 34 GENIC homozygous 806123910 1 263815026 263815027 C T 61 GENIC homozygous 806123911 1 263815349 263815350 G A 50 GENIC homozygous 806123912 1 263815744 263815745 A G 51 GENIC homozygous 806123913 1 263817320 263817321 G A 61 GENIC homozygous 806123914 1 263817743 263817744 A G 54 GENIC homozygous 806123915 1 263818715 263818716 G A 53 GENIC homozygous 806123916 1 263820712 263820713 T C 44 GENIC homozygous 806123917 1 263820813 263820814 A G 65 GENIC homozygous 806123918 1 263820861 263820862 C T 62 GENIC homozygous 806123919 1 263823243 263823244 C T 59 GENIC homozygous 806123920 1 263825226 263825227 C T 43 GENIC heterozygous 806123921 1 263825765 263825766 G T 34 GENIC possibly homozygous 806123922 1 263826119 263826120 G A 56 GENIC homozygous 806123923 1 263827331 263827332 G A 52 GENIC possibly homozygous 806123924 1 263828502 263828503 C A 50 GENIC possibly homozygous 806123925 1 263830697 263830698 G A 40 GENIC homozygous 806123926 1 263831722 263831723 C T 39 GENIC homozygous 806123927 1 263832813 263832814 A G 33 GENIC homozygous 806123928 1 263835278 263835279 C T 59 GENIC homozygous 806123929 1 263835926 263835927 G A 50 GENIC homozygous 806123930 1 263840399 263840400 G A 30 GENIC homozygous 806123931 1 263843300 263843301 A T 40 GENIC homozygous 806123932