chr start stop reference nuc variant nuc depth genic status zygosity variant ID 10 82131319 82131320 G - 11 GENIC homozygous 51516668 10 82131346 82131347 C - 16 GENIC homozygous 51516669 10 82138978 82138979 G T 7 GENIC homozygous 51516720 10 82138983 82138984 C T 8 GENIC homozygous 51516721 10 82138998 82138999 G T 8 GENIC homozygous 51516722 10 82139000 82139001 A T 8 GENIC homozygous 51516723 10 82139007 82139008 A T 9 GENIC homozygous 51516724 10 82139019 82139020 A T 12 GENIC homozygous 51516725 10 82139258 82139259 C G 11 GENIC homozygous 51516729 10 82139262 82139263 A AG 10 GENIC homozygous 51516730 10 82139268 82139269 A - 10 GENIC homozygous 51516731 10 82133626 82133627 A - 11 GENIC homozygous 53530158 10 82155032 82155033 T - 11 GENIC heterozygous 51516783 10 82159768 82159772 ATTT ---- 7 GENIC homozygous 51717191 10 82161459 82161460 G A 24 INTERGENIC heterozygous 51516799 10 82161678 82161679 T - 25 INTERGENIC heterozygous 52390730 10 82161678 82161679 T C 25 INTERGENIC heterozygous 53530159 10 82161681 82161682 T C 28 INTERGENIC heterozygous 53530160 10 82161930 82161931 T C 18 INTERGENIC heterozygous 53530161 10 82180640 82180641 T - 11 GENIC heterozygous 51717237 10 82185481 82185482 C CA 11 GENIC homozygous 51516834