chr start stop reference nuc variant nuc depth genic status zygosity variant ID 3 123454486 123454487 A G 25 GENIC homozygous 984769527 3 123466525 123466526 A G 11 GENIC homozygous 984769528 3 123468702 123468703 A G 22 GENIC homozygous 984769529 3 123476583 123476584 A T 38 GENIC homozygous 984769530 3 123476589 123476590 A T 33 GENIC homozygous 984769531 3 123476592 123476593 C T 32 GENIC homozygous 984769532 3 123476598 123476599 G T 33 GENIC homozygous 984769533 3 123476606 123476607 G T 35 GENIC homozygous 984769534 3 123476609 123476610 C A 35 GENIC homozygous 984769535 3 123476623 123476624 G A 33 GENIC homozygous 984769536 3 123476627 123476628 G C 34 GENIC homozygous 984769537 3 123476632 123476633 T A 33 GENIC homozygous 984769538 3 123476680 123476681 C G 36 GENIC homozygous 984769539 3 123476690 123476691 G A 34 GENIC homozygous 984769540 3 123476718 123476719 T G 32 GENIC homozygous 984769541 3 123476726 123476727 T G 28 GENIC homozygous 984769542 3 123493789 123493790 G A 20 GENIC homozygous 984769543 3 123494469 123494470 A C 20 GENIC homozygous 984769544 3 123504390 123504391 A G 19 GENIC homozygous 984769545 3 123507546 123507547 C G 31 GENIC homozygous 984769546 3 123508327 123508328 G C 20 GENIC homozygous 984769547 3 123512363 123512364 C A 25 GENIC homozygous 984769548 3 123514916 123514917 C T 15 GENIC homozygous 984769549 3 123547831 123547832 T G 19 GENIC homozygous 984769550 3 123550770 123550771 T A 7 GENIC homozygous 984769551 3 123551045 123551046 C T 5 GENIC homozygous 984769552 3 123561603 123561604 G C 7 GENIC homozygous 984769553