chr start stop reference nuc variant nuc depth genic status zygosity variant ID 10 82131319 82131320 G - 3 GENIC homozygous 51516668 10 82131346 82131347 C - 1 GENIC homozygous 51516669 10 82133627 82133628 A - 11 GENIC homozygous 52068528 10 82134495 82134496 G T 6 GENIC homozygous 51516690 10 82138961 82138962 G T 11 GENIC homozygous 52390726 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 13 GENIC homozygous 51516723 10 82139007 82139008 A T 13 GENIC homozygous 51516724 10 82139019 82139020 A T 14 GENIC homozygous 51516725 10 82139258 82139259 C G 8 GENIC homozygous 51516729 10 82139262 82139263 A AG 8 GENIC homozygous 51516730 10 82139268 82139269 A - 7 GENIC homozygous 51516731 10 82140058 82140059 C CT 3 GENIC heterozygous 52461988 10 82140059 82140061 TT -- 3 GENIC heterozygous 51717142 10 82144586 82144588 CA -- 2 GENIC homozygous 51516752 10 82151167 82151168 A - 11 INTERGENIC heterozygous 52506282 10 82159768 82159772 ATTT ---- 1 GENIC homozygous 51717191 10 82160390 82160391 T G 2 INTERGENIC homozygous 51516792 10 82160391 82160392 T A 2 INTERGENIC homozygous 51516793 10 82160396 82160397 C - 3 INTERGENIC homozygous 51516794 10 82160397 82160398 C G 3 INTERGENIC homozygous 52390728 10 82161615 82161616 G - 11 INTERGENIC heterozygous 51516802 10 82177767 82177768 C CT 3 GENIC heterozygous 52390732 10 82180640 82180641 T - 2 GENIC heterozygous 51717237 10 82185481 82185482 C CA 8 GENIC homozygous 51516834