chr start stop reference nuc variant nuc depth genic status zygosity variant ID 1 263812471 263812472 G A 26 GENIC homozygous 954111635 1 263813164 263813165 C A 29 GENIC homozygous 954111636 1 263813314 263813315 G A 24 GENIC homozygous 954111637 1 263813492 263813493 T A 38 GENIC homozygous 954111638 1 263814051 263814052 C T 26 GENIC homozygous 954111639 1 263815744 263815745 A G 22 GENIC homozygous 954111640 1 263817743 263817744 A G 31 GENIC homozygous 954111641 1 263820813 263820814 A G 31 GENIC homozygous 954111642 1 263820861 263820862 C T 34 GENIC homozygous 954111643 1 263821401 263821402 G A 20 GENIC homozygous 954111644 1 263823231 263823232 G A 35 GENIC homozygous 954111645 1 263823243 263823244 C T 34 GENIC homozygous 954111646 1 263823512 263823513 A G 24 GENIC homozygous 954111647 1 263825765 263825766 G T 9 GENIC homozygous 954111648 1 263827331 263827332 G A 23 GENIC homozygous 954111649 1 263828502 263828503 C A 27 GENIC homozygous 954111650 1 263831722 263831723 C T 24 GENIC homozygous 954111651 1 263832115 263832116 T C 17 GENIC homozygous 954111652 1 263832813 263832814 A G 17 GENIC homozygous 954111653 1 263835278 263835279 C T 26 GENIC homozygous 954111654 1 263835926 263835927 G A 20 GENIC homozygous 954111655 1 263837493 263837494 G A 25 GENIC homozygous 954111656 1 263840846 263840847 C T 30 GENIC homozygous 954111657 1 263842282 263842283 G T 41 GENIC possibly homozygous 954111658 1 263843300 263843301 A T 28 GENIC homozygous 954111659 1 263844963 263844964 A G 26 GENIC homozygous 954111660