chr start stop reference nuc variant nuc depth genic status zygosity variant ID 10 82131319 82131320 G - 1 GENIC homozygous 51516668 10 82131346 82131347 C - 2 GENIC homozygous 51516669 10 82137690 82137691 C - 2 GENIC heterozygous 51516710 10 82138978 82138979 G T 1 GENIC homozygous 51516720 10 82138983 82138984 C T 1 GENIC homozygous 51516721 10 82138998 82138999 G T 1 GENIC homozygous 51516722 10 82139000 82139001 A T 1 GENIC homozygous 51516723 10 82139007 82139008 A T 3 GENIC homozygous 51516724 10 82139019 82139020 A T 10 GENIC homozygous 51516725 10 82139171 82139172 A - 5 GENIC heterozygous 51516727 10 82139195 82139196 A - 1 GENIC homozygous 51516728 10 82138961 82138962 G T 1 GENIC homozygous 52390726 10 82160390 82160391 T G 1 INTERGENIC homozygous 51516792 10 82160391 82160392 T A 1 INTERGENIC homozygous 51516793 10 82160396 82160397 C - 1 INTERGENIC homozygous 51516794 10 82160397 82160398 C G 1 INTERGENIC homozygous 52390728 10 82185481 82185482 C CA 22 GENIC possibly homozygous 51516834 10 82152291 82152292 A - 2 INTERGENIC heterozygous 52322206