chr start stop reference nuc variant nuc depth genic status zygosity variant ID 17 80431215 80431216 T C 28 GENIC possibly homozygous 673069339 17 80435350 80435351 A AACCTGCCTGTCCCCGG 11 GENIC heterozygous 769977089 17 80437278 80437279 C CT 23 GENIC heterozygous 769977090 17 80437514 80437515 T TAAAAA 6 GENIC heterozygous 769977091 17 80438906 80438907 G GT 42 GENIC homozygous 769977092 17 80440935 80440936 C CAAAAAAAAAA 5 GENIC heterozygous 769977094 17 80441585 80441586 A G 8 GENIC heterozygous 673069340 17 80442233 80442234 G GGAGGTGGGAGAGAGGTGGGAGGTGGGAGGTGGGAGGTGGGAGA 2 GENIC heterozygous 769977095 17 80444630 80444631 C CA 19 GENIC heterozygous 769977096 17 80444659 80444660 G GCA 5 GENIC heterozygous 769977098 17 80449799 80449810 TTTTTTTTTTT ----------- 12 GENIC possibly homozygous 769977099 17 80450841 80450842 T TTGTG 7 GENIC possibly homozygous 769977102 17 80452760 80452761 T TC 42 GENIC heterozygous 769977103 17 80452781 80452782 G A 41 GENIC heterozygous 673069341 17 80452786 80452787 G A 40 GENIC heterozygous 673069342 17 80454135 80454136 C T 20 GENIC heterozygous 673069343 17 80454265 80454266 T - 19 GENIC heterozygous 769977104