chr start stop reference nuc variant nuc depth genic status zygosity variant ID 8 103778966 103778967 G 11 GENIC homozygous 128623608 8 103779373 103779374 T A 15 GENIC homozygous 116618921 8 103780270 103780271 T C 8 GENIC homozygous 116618933 8 103792107 103792108 T G 4 GENIC homozygous 116618947 8 103792110 103792110 A 4 GENIC homozygous 129950657 8 103808378 103808380 TC 7 GENIC heterozygous 130672753 8 103827996 103827996 TGGT 6 GENIC homozygous 131052711 8 103835413 103835414 C G 11 GENIC homozygous 116984562 8 103835418 103835419 A G 11 GENIC homozygous 116984563 8 103847285 103847286 A G 8 GENIC possibly homozygous 116984564 8 103846100 103846101 G C 17 GENIC heterozygous 131061067 8 103846104 103846105 G A 17 GENIC heterozygous 128665422 8 103846105 103846106 T C 16 GENIC heterozygous 128665423 8 103849635 103849636 G A 10 GENIC heterozygous 131061068 8 103881255 103881256 A C 17 GENIC homozygous 116619156