chr start stop reference nuc variant nuc depth genic status zygosity variant ID 10 82131319 82131320 G - 9 GENIC homozygous 51516668 10 82131346 82131347 C - 9 GENIC homozygous 51516669 10 82134495 82134496 G T 14 GENIC possibly homozygous 51516690 10 82137690 82137691 C - 5 GENIC homozygous 51516710 10 82138978 82138979 G T 18 GENIC homozygous 51516720 10 82138983 82138984 C T 19 GENIC homozygous 51516721 10 82138998 82138999 G T 20 GENIC homozygous 51516722 10 82139000 82139001 A T 20 GENIC homozygous 51516723 10 82139007 82139008 A T 22 GENIC homozygous 51516724 10 82139019 82139020 A T 22 GENIC homozygous 51516725 10 82139195 82139196 A - 9 GENIC heterozygous 51516728 10 82139258 82139259 C G 13 GENIC homozygous 51516729 10 82139262 82139263 A AG 13 GENIC homozygous 51516730 10 82139268 82139269 A - 13 GENIC homozygous 51516731 10 82143917 82143918 T - 14 GENIC heterozygous 51516747 10 82138961 82138962 G T 13 GENIC homozygous 52390726 10 82147653 82147654 T - 14 INTERGENIC heterozygous 52461990 10 82151167 82151168 A - 7 INTERGENIC heterozygous 52506282 10 82160390 82160391 T G 20 INTERGENIC homozygous 51516792 10 82160391 82160392 T A 20 INTERGENIC homozygous 51516793 10 82160396 82160397 C - 20 INTERGENIC homozygous 51516794 10 82160397 82160398 C G 20 INTERGENIC homozygous 52390728 10 82161615 82161616 G - 21 INTERGENIC heterozygous 51516802 10 82170321 82170325 TATG ---- 17 INTERGENIC homozygous 51717210 10 82177767 82177768 C CT 4 GENIC heterozygous 52390732 10 82185481 82185482 C CA 11 GENIC homozygous 51516834