chr start stop reference nuc variant nuc depth genic status zygosity variant ID 9 15544354 15544355 C T 48 GENIC possibly homozygous 533856137 9 15544757 15544758 T C 51 GENIC possibly homozygous 533856138 9 15544874 15544879 CCCCC ----- 14 GENIC heterozygous 695953060 9 15544877 15544879 CC -- 14 GENIC heterozygous 695953061 9 15544886 15544890 CCCA ---- 16 GENIC homozygous 695953062 9 15545169 15545170 C CT 17 GENIC possibly homozygous 695953063 9 15545194 15545195 C T 32 GENIC possibly homozygous 533856139 9 15545224 15545225 G A 29 GENIC possibly homozygous 533856140 9 15545594 15545595 G A 35 GENIC homozygous 533856141 9 15545951 15545952 C CCA 42 GENIC homozygous 695953064 9 15545987 15545988 A G 48 GENIC homozygous 533856142 9 15546345 15546346 C G 26 GENIC possibly homozygous 533856143 9 15546652 15546653 A G 45 GENIC homozygous 533856144 9 15546932 15546933 G A 38 GENIC possibly homozygous 533856145 9 15546996 15546997 A C 50 GENIC homozygous 533856146 9 15547034 15547035 A G 56 GENIC homozygous 533856147 9 15548075 15548076 G GAC 17 GENIC possibly homozygous 695953065 9 15548120 15548121 C A 32 GENIC homozygous 533856148 9 15548312 15548313 A G 23 GENIC homozygous 533856149 9 15548532 15548533 T C 35 GENIC homozygous 533856150