chr start stop reference nuc variant nuc depth genic status zygosity variant ID 10 111309537 111309538 A T 109 GENIC heterozygous 507633432 10 111311177 111311178 T C 72 GENIC heterozygous 510626648 10 111311394 111311395 T C 95 GENIC heterozygous 510626649 10 111311447 111311448 T C 87 GENIC heterozygous 510626650 10 111311501 111311502 T C 63 GENIC heterozygous 510626651 10 111311517 111311518 A C 54 GENIC heterozygous 510626652 10 111311526 111311527 C T 58 GENIC heterozygous 510626653 10 111311567 111311568 G A 59 GENIC heterozygous 510626654 10 111311614 111311615 A G 48 GENIC heterozygous 510626655 10 111318895 111318896 C G 92 GENIC heterozygous 507633433 10 111318966 111318967 T - 94 GENIC heterozygous 686162633 10 111318994 111318995 A C 98 GENIC heterozygous 507633434 10 111320871 111320872 T C 96 GENIC heterozygous 510626656 10 111320895 111320896 G A 108 GENIC heterozygous 510626657 10 111320944 111320945 T A 107 GENIC heterozygous 510626658 10 111320961 111320962 G T 95 GENIC heterozygous 510626659 10 111321297 111321298 A T 69 GENIC heterozygous 510626660 10 111321330 111321331 G C 72 GENIC heterozygous 510626661 10 111321754 111321755 C A 109 GENIC heterozygous 510626662 10 111321845 111321846 G A 144 GENIC heterozygous 510626663 10 111322101 111322102 G T 80 GENIC heterozygous 510626664