chr start stop reference nuc variant nuc depth genic status zygosity variant ID 13 25930171 25930172 C T 27 GENIC homozygous 947933014 13 25933968 25933969 A G 16 GENIC homozygous 947933015 13 25934410 25934411 C T 20 GENIC homozygous 947933016 13 25935151 25935152 C T 22 GENIC homozygous 947933017 13 25936981 25936982 C G 2 GENIC homozygous 947933018 13 25940180 25940181 C A 17 GENIC homozygous 947933019 13 25940369 25940370 G A 21 GENIC homozygous 947933020 13 25941095 25941096 T C 24 GENIC homozygous 947933021 13 25941195 25941196 C A 23 GENIC homozygous 947933022 13 25941208 25941209 C T 25 GENIC homozygous 947933023 13 25941736 25941737 A G 25 GENIC homozygous 947933024 13 25944571 25944572 A C 11 GENIC homozygous 947933025 13 25948655 25948656 T C 20 GENIC homozygous 947933026 13 25949735 25949736 G A 30 GENIC homozygous 947933027 13 25950017 25950018 T C 28 GENIC homozygous 947933028 13 25950113 25950114 G A 21 GENIC homozygous 947933029 13 25950170 25950171 G A 21 GENIC homozygous 947933030 13 25951505 25951506 G A 24 GENIC homozygous 947933031 13 25952526 25952527 G A 23 GENIC homozygous 947933032