chr start stop reference nuc variant nuc depth genic status zygosity variant ID 10 105568153 105568154 A G 20 GENIC homozygous 116837132 10 105568214 105568215 A T 21 GENIC homozygous 116837134 10 105568539 105568540 A G 20 GENIC homozygous 116837136 10 105568777 105568778 T C 15 GENIC homozygous 116837138 10 105569180 105569181 C G 18 GENIC homozygous 116837140 10 105569232 105569233 T C 21 GENIC homozygous 116837142 10 105569499 105569500 C T 16 GENIC homozygous 116837144 10 105569518 105569519 A G 17 GENIC homozygous 116837146 10 105569583 105569584 C T 22 GENIC homozygous 116837148 10 105569639 105569640 G A 23 GENIC homozygous 116837150 10 105569650 105569651 C T 23 GENIC homozygous 116837152 10 105569707 105569708 T C 22 GENIC homozygous 116837154 10 105570831 105570832 T C 21 GENIC homozygous 116837156 10 105571011 105571012 G A 22 GENIC homozygous 116837158 10 105571015 105571016 G A 21 GENIC homozygous 116837160 10 105572049 105572050 G T 20 GENIC homozygous 116837162 10 105572123 105572124 C G 17 GENIC homozygous 116837164 10 105572362 105572363 T C 16 GENIC homozygous 116837166 10 105570721 105570722 G A 15 GENIC homozygous 117279828