chr start stop reference nuc variant nuc depth genic status zygosity variant ID 12 38095835 38095836 A C 28 GENIC possibly homozygous 813445607 12 38096899 38096900 T G 7 GENIC heterozygous 813445608 12 38096954 38096955 G C 15 GENIC homozygous 813445609 12 38100973 38100974 G C 36 GENIC homozygous 813445610 12 38101113 38101114 G A 16 GENIC homozygous 813445611 12 38101123 38101124 G T 13 GENIC homozygous 813445612 12 38103175 38103176 A C 39 GENIC homozygous 813445613 12 38103344 38103345 A C 21 GENIC homozygous 813445614 12 38104417 38104418 A T 20 GENIC homozygous 813445615 12 38104891 38104892 G C 26 GENIC homozygous 813445616 12 38106139 38106140 C T 15 GENIC possibly homozygous 813445617 12 38106408 38106409 G A 22 GENIC homozygous 813445618 12 38106726 38106727 A G 25 GENIC homozygous 813445619 12 38110578 38110579 A G 29 GENIC homozygous 813445620 12 38110996 38110997 G A 27 GENIC homozygous 813445621 12 38113923 38113924 G C 10 GENIC homozygous 813445622 12 38113945 38113946 T C 8 GENIC homozygous 813445623 12 38114516 38114517 A T 27 GENIC homozygous 813445624 12 38116443 38116444 C T 23 GENIC possibly homozygous 813445625