chr start stop reference nuc variant nuc depth genic status zygosity variant ID 13 89726258 89726259 G A 13 GENIC homozygous 890526076 13 89727003 89727004 C T 7 GENIC homozygous 890526077 13 89727289 89727290 C T 13 GENIC homozygous 890526078 13 89728199 89728200 A G 27 GENIC homozygous 890526079 13 89728283 89728284 G A 14 GENIC homozygous 890526080 13 89728524 89728525 A G 8 GENIC homozygous 890526081 13 89728997 89728998 A G 3 GENIC heterozygous 890526082 13 89729103 89729104 G A 21 GENIC homozygous 890526083 13 89730067 89730068 G A 16 GENIC homozygous 890526084 13 89735314 89735315 T C 20 GENIC homozygous 890526085 13 89736067 89736068 G C 22 GENIC homozygous 890526086 13 89736970 89736971 A T 19 GENIC homozygous 890526087 13 89738441 89738442 C G 26 GENIC homozygous 890526088 13 89740874 89740875 T C 24 GENIC homozygous 890526089 13 89740981 89740982 T G 13 GENIC homozygous 890526090 13 89741383 89741384 C G 7 GENIC homozygous 890526091 13 89742437 89742438 C T 29 GENIC homozygous 890526092