chr start stop reference nuc variant nuc depth genic status zygosity variant ID 20 3554097 3554098 T G 15 GENIC homozygous 109069052 20 3557322 3557323 G T 6 GENIC homozygous 109069056 20 3557368 3557369 C T 6 GENIC homozygous 109069058 20 3557546 3557547 A T 16 GENIC homozygous 109069060 20 3558080 3558081 T C 30 GENIC homozygous 109069062 20 3558518 3558519 G A 26 GENIC homozygous 109069064 20 3561290 3561291 C T 19 GENIC homozygous 109069068 20 3561391 3561392 A G 20 GENIC homozygous 109069070 20 3562750 3562751 C T 15 GENIC homozygous 109069072 20 3562751 3562752 C T 15 GENIC homozygous 109069074 20 3564434 3564435 T C 27 GENIC homozygous 109069076 20 3564691 3564692 C T 20 GENIC homozygous 109069078 20 3567270 3567271 G A 8 GENIC homozygous 109069080 20 3567637 3567638 A G 3 GENIC homozygous 109069082 20 3568323 3568324 T G 14 GENIC homozygous 109069084 20 3570271 3570272 T C 20 GENIC homozygous 109069086 20 3570393 3570394 A G 17 GENIC homozygous 109069088 20 3573009 3573010 T G 16 GENIC homozygous 109069090 20 3573300 3573301 C A 27 GENIC homozygous 109069092 20 3573647 3573648 G A 18 GENIC homozygous 109069095 20 3573929 3573930 C T 15 GENIC homozygous 109069097 20 3574212 3574213 C T 7 GENIC homozygous 109069099