chr start stop reference nuc variant nuc depth genic status zygosity variant ID 16 24863113 24863114 C CGT 5 GENIC homozygous 745092686 16 24863132 24863133 T A 11 GENIC homozygous 629702059 16 24863203 24863204 T A 14 GENIC possibly homozygous 629702060 16 24863761 24863762 G A 29 GENIC possibly homozygous 629702061 16 24863891 24863892 G C 12 GENIC homozygous 629702062 16 24863990 24863991 G GT 6 GENIC heterozygous 745092687 16 24865275 24865276 A - 17 GENIC homozygous 745092688 16 24865616 24865617 C T 11 GENIC heterozygous 629702063 16 24866700 24866701 T C 7 GENIC homozygous 629702064 16 24866802 24866803 C T 18 GENIC possibly homozygous 629702065 16 24867027 24867028 C CT 14 GENIC homozygous 745092689 16 24867757 24867758 A G 18 GENIC possibly homozygous 629702066 16 24868550 24868551 C T 20 GENIC heterozygous 629702067 16 24869187 24869188 C T 15 GENIC homozygous 629702068 16 24869201 24869202 G A 14 GENIC homozygous 629702069 16 24869407 24869408 T A 25 GENIC possibly homozygous 629702070 16 24869649 24869653 TAAG ---- 8 GENIC homozygous 745092690 16 24869717 24869718 G C 21 GENIC homozygous 629702071 16 24869748 24869749 A - 14 GENIC homozygous 745092691 16 24870274 24870275 C G 24 GENIC homozygous 629702072 16 24871355 24871356 C G 11 GENIC possibly homozygous 629702073 16 24871699 24871700 C T 7 GENIC homozygous 629702074 16 24871737 24871738 C A 5 GENIC homozygous 629702075