chr start stop reference nuc variant nuc depth genic status zygosity variant ID 10 82129580 82129582 AG -- 9 GENIC heterozygous 52444010 10 82131319 82131320 G - 18 GENIC homozygous 51516668 10 82131346 82131347 C - 17 GENIC homozygous 51516669 10 82133627 82133628 A - 12 GENIC homozygous 52068528 10 82134495 82134496 G T 11 GENIC homozygous 51516690 10 82137690 82137691 C - 3 GENIC heterozygous 51516710 10 82138978 82138979 G T 14 GENIC homozygous 51516720 10 82138983 82138984 C T 14 GENIC homozygous 51516721 10 82138998 82138999 G T 13 GENIC homozygous 51516722 10 82139000 82139001 A T 14 GENIC homozygous 51516723 10 82139007 82139008 A T 14 GENIC homozygous 51516724 10 82139019 82139020 A T 16 GENIC homozygous 51516725 10 82139258 82139259 C G 21 GENIC homozygous 51516729 10 82139262 82139263 A AG 21 GENIC homozygous 51516730 10 82139268 82139269 A - 21 GENIC homozygous 51516731 10 82144586 82144588 CA -- 4 GENIC heterozygous 51516752 10 82138961 82138962 G T 13 GENIC homozygous 52390726 10 82151193 82151194 C CAAA 10 INTERGENIC heterozygous 52444012 10 82155032 82155033 T - 10 GENIC heterozygous 51516783 10 82160390 82160391 T G 21 INTERGENIC homozygous 51516792 10 82160391 82160392 T A 21 INTERGENIC homozygous 51516793 10 82160396 82160397 C - 22 INTERGENIC homozygous 51516794 10 82160397 82160398 C G 20 INTERGENIC homozygous 52390728 10 82161615 82161616 G - 37 INTERGENIC heterozygous 51516802 10 82161678 82161679 T - 29 INTERGENIC heterozygous 52390730 10 82161820 82161821 G GACACCTCTGTCTCC 12 INTERGENIC heterozygous 51516803 10 82163953 82163957 AACC ---- 22 INTERGENIC heterozygous 52444014 10 82163975 82163976 C T 19 INTERGENIC heterozygous 51516809 10 82164415 82164416 A - 5 INTERGENIC heterozygous 52068562 10 82164437 82164438 C CT 4 INTERGENIC heterozygous 52444016 10 82164438 82164439 T - 4 INTERGENIC heterozygous 51516812 10 82177767 82177768 C CT 6 GENIC heterozygous 52390732 10 82185481 82185482 C CA 21 GENIC homozygous 51516834