chr start stop reference nuc variant nuc depth genic status zygosity variant ID 20 3974272 3974273 T C 32 GENIC homozygous 971381362 20 3974455 3974456 C T 32 GENIC homozygous 971381363 20 3974584 3974585 A G 32 GENIC homozygous 971381364 20 3974590 3974591 T C 31 GENIC homozygous 971381365 20 3974653 3974654 A G 36 GENIC homozygous 971381366 20 3974780 3974781 T C 37 GENIC homozygous 971381367 20 3974895 3974896 C G 36 GENIC homozygous 971381368 20 3975624 3975625 G A 41 GENIC homozygous 971381369 20 3975687 3975688 C G 43 GENIC homozygous 971381370 20 3975807 3975808 G A 21 GENIC homozygous 971381371 20 3975840 3975841 A G 24 GENIC homozygous 971381372 20 3976062 3976063 G A 35 GENIC possibly homozygous 971381373 20 3976179 3976180 A G 29 GENIC homozygous 971381374 20 3976620 3976621 G T 31 GENIC homozygous 971381375 20 3976662 3976663 C T 37 GENIC homozygous 971381376 20 3976690 3976691 G A 32 GENIC homozygous 971381377 20 3976750 3976751 T A 30 GENIC homozygous 971381378 20 3976751 3976752 T C 30 GENIC homozygous 971381379 20 3976783 3976784 A C 30 GENIC homozygous 971381380 20 3976884 3976885 G A 24 GENIC homozygous 971381381 20 3976982 3976983 C A 41 GENIC homozygous 971381382 20 3976998 3976999 A G 42 GENIC homozygous 971381383 20 3977048 3977049 G A 44 GENIC homozygous 971381384 20 3977163 3977164 C T 34 GENIC homozygous 971381385 20 3977906 3977907 C T 37 GENIC homozygous 971381386 20 3978365 3978366 G A 18 GENIC homozygous 971381387 20 3978406 3978407 G T 24 GENIC homozygous 971381388 20 3978609 3978610 C T 28 GENIC homozygous 971381389