chr start stop reference nuc variant nuc depth genic status zygosity variant ID 13 25929592 25929593 G C 14 GENIC homozygous 973593120 13 25930014 25930015 C G 13 GENIC homozygous 973593121 13 25933968 25933969 A G 25 GENIC homozygous 973593122 13 25934709 25934710 G T 29 GENIC homozygous 973593123 13 25935708 25935709 C T 18 GENIC homozygous 973593124 13 25935922 25935923 G A 17 GENIC homozygous 973593125 13 25939690 25939691 C T 14 GENIC homozygous 973593126 13 25940180 25940181 C A 7 GENIC homozygous 973593127 13 25940369 25940370 G A 17 GENIC homozygous 973593128 13 25941095 25941096 T C 19 GENIC homozygous 973593129 13 25941195 25941196 C A 16 GENIC homozygous 973593130 13 25941208 25941209 C T 19 GENIC homozygous 973593131 13 25941736 25941737 A G 26 GENIC homozygous 973593132 13 25942084 25942085 C T 13 GENIC homozygous 973593133 13 25943081 25943082 G A 21 GENIC homozygous 973593134 13 25945548 25945549 C T 17 GENIC homozygous 973593135 13 25947683 25947684 C G 7 GENIC homozygous 973593136 13 25949824 25949825 T A 25 GENIC homozygous 973593137 13 25951557 25951558 G A 16 GENIC homozygous 973593138