chr start stop reference nuc variant nuc depth genic status zygosity variant ID 10 111309785 111309786 G A 18 GENIC heterozygous 512186036 10 111309838 111309839 T G 33 GENIC heterozygous 515115440 10 111311177 111311178 T C 66 GENIC heterozygous 515115441 10 111311394 111311395 T C 135 GENIC heterozygous 515115442 10 111311460 111311461 C T 137 GENIC heterozygous 515115443 10 111311517 111311518 A C 126 GENIC heterozygous 515115444 10 111311526 111311527 C T 122 GENIC heterozygous 515115445 10 111311567 111311568 G A 113 GENIC heterozygous 515115446 10 111311614 111311615 A G 106 GENIC heterozygous 515115447 10 111318895 111318896 C G 21 GENIC heterozygous 512186037 10 111318994 111318995 A C 11 GENIC heterozygous 512186038 10 111320529 111320530 A G 32 GENIC heterozygous 515115448 10 111320871 111320872 T C 29 GENIC heterozygous 515115449 10 111320895 111320896 G A 32 GENIC heterozygous 515115450 10 111320944 111320945 T A 34 GENIC heterozygous 515115451 10 111320961 111320962 G T 34 GENIC heterozygous 515115452 10 111321173 111321174 A G 30 GENIC heterozygous 515115453 10 111321297 111321298 A T 27 GENIC heterozygous 515115454 10 111321330 111321331 G C 33 GENIC heterozygous 515115455 10 111321553 111321554 T G 38 GENIC heterozygous 515115456 10 111322054 111322055 C A 40 GENIC heterozygous 515115457 10 111322057 111322058 A T 39 GENIC heterozygous 515115458 10 111322101 111322102 G T 38 GENIC heterozygous 515115459