chr start stop reference nuc variant nuc depth genic status zygosity variant ID 13 25929592 25929593 G C 24 GENIC homozygous 988963231 13 25933968 25933969 A G 21 GENIC homozygous 988963232 13 25934709 25934710 G T 30 GENIC homozygous 988963233 13 25935708 25935709 C T 16 GENIC homozygous 988963234 13 25935922 25935923 G A 33 GENIC homozygous 988963235 13 25939690 25939691 C T 32 GENIC homozygous 988963236 13 25939981 25939982 C G 5 GENIC homozygous 988963237 13 25940180 25940181 C A 16 GENIC homozygous 988963238 13 25940369 25940370 G A 4 GENIC homozygous 988963239 13 25941095 25941096 T C 19 GENIC homozygous 988963240 13 25941195 25941196 C A 18 GENIC homozygous 988963241 13 25941208 25941209 C T 18 GENIC homozygous 988963242 13 25941736 25941737 A G 19 GENIC homozygous 988963243 13 25942084 25942085 C T 20 GENIC homozygous 988963244 13 25943081 25943082 G A 58 GENIC homozygous 988963245 13 25945548 25945549 C T 37 GENIC homozygous 988963246 13 25947683 25947684 C G 8 GENIC homozygous 988963247 13 25949824 25949825 T A 20 GENIC homozygous 988963248