chr start stop reference nuc variant nuc depth genic status zygosity variant ID 10 82131346 82131347 C - 1 GENIC homozygous 51516669 10 82133627 82133628 A - 7 GENIC possibly homozygous 52068528 10 82137690 82137691 C - 4 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 1 GENIC homozygous 51516724 10 82139019 82139020 A T 4 GENIC homozygous 51516725 10 82139171 82139172 A - 7 GENIC heterozygous 51516727 10 82139258 82139259 C G 2 GENIC homozygous 51516729 10 82139262 82139263 A AG 2 GENIC heterozygous 51516730 10 82139268 82139269 A - 4 GENIC heterozygous 51516731 10 82138961 82138962 G T 2 GENIC homozygous 52390726 10 82151061 82151063 AC -- 6 INTERGENIC heterozygous 52068545 10 82155032 82155033 T - 1 GENIC homozygous 51516783 10 82163953 82163957 AACC ---- 20 INTERGENIC heterozygous 52444014 10 82163975 82163976 C T 14 INTERGENIC heterozygous 51516809 10 82185481 82185482 C CA 20 GENIC possibly homozygous 51516834 10 82188536 82188537 C - 6 GENIC heterozygous 52570465