chr start stop reference nuc variant nuc depth genic status zygosity variant ID 20 3974272 3974273 T C 26 GENIC homozygous 948655485 20 3974455 3974456 C T 18 GENIC homozygous 948655486 20 3974584 3974585 A G 20 GENIC homozygous 948655487 20 3974590 3974591 T C 19 GENIC homozygous 948655488 20 3974653 3974654 A G 15 GENIC homozygous 948655489 20 3974780 3974781 T C 12 GENIC homozygous 948655490 20 3974895 3974896 C G 16 GENIC homozygous 948655491 20 3975624 3975625 G A 22 GENIC possibly homozygous 948655492 20 3975687 3975688 C G 25 GENIC possibly homozygous 948655493 20 3975807 3975808 G A 27 GENIC homozygous 948655494 20 3975840 3975841 A G 27 GENIC homozygous 948655495 20 3976062 3976063 G A 14 GENIC homozygous 948655496 20 3976179 3976180 A G 13 GENIC homozygous 948655497 20 3976499 3976500 G A 20 GENIC homozygous 948655498 20 3976620 3976621 G T 31 GENIC homozygous 948655499 20 3976662 3976663 C T 30 GENIC homozygous 948655500 20 3976690 3976691 G A 22 GENIC homozygous 948655501 20 3976750 3976751 T A 21 GENIC homozygous 948655502 20 3976751 3976752 T C 21 GENIC homozygous 948655503 20 3976783 3976784 A C 26 GENIC homozygous 948655504 20 3976884 3976885 G A 28 GENIC homozygous 948655505 20 3976982 3976983 C A 28 GENIC homozygous 948655506 20 3976998 3976999 A G 25 GENIC homozygous 948655507 20 3977048 3977049 G A 30 GENIC homozygous 948655508 20 3977163 3977164 C T 25 GENIC homozygous 948655509 20 3977906 3977907 C T 27 GENIC homozygous 948655510 20 3978365 3978366 G A 13 GENIC homozygous 948655511 20 3978406 3978407 G T 22 GENIC homozygous 948655512 20 3978609 3978610 C T 21 GENIC homozygous 948655513