chr start stop reference nuc variant nuc depth genic status zygosity variant ID 2 66601486 66601487 C T 20 GENIC homozygous 110702251 2 66601609 66601610 A T 16 GENIC homozygous 109801023 2 66601817 66601818 G A 20 GENIC homozygous 109801026 2 66601865 66601866 T C 23 GENIC homozygous 109801028 2 66607502 66607503 C A 44 GENIC heterozygous 109801032 2 66607615 66607616 A G 42 GENIC homozygous 109801034 2 66607641 66607642 T A 42 GENIC heterozygous 109801036 2 66609082 66609083 T C 15 GENIC homozygous 109801049 2 66609314 66609315 C A 22 GENIC homozygous 111247420 2 66609367 66609368 A G 22 GENIC homozygous 109801051 2 66609571 66609572 A G 21 GENIC homozygous 111247424 2 66610098 66610099 C T 20 GENIC homozygous 111247426 2 66612267 66612268 A G 31 GENIC homozygous 109801084 2 66612298 66612299 A G 22 GENIC homozygous 111247432 2 66612326 66612327 G A 22 GENIC homozygous 111247434 2 66613791 66613792 C T 39 GENIC possibly homozygous 111247440 2 66614326 66614327 G C 20 GENIC homozygous 109801101 2 66614674 66614675 G T 32 GENIC homozygous 111247450 2 66611032 66611033 G A 14 GENIC possibly homozygous 120437290