chr start stop reference nuc variant nuc depth genic status zygosity variant ID 19 56010732 56010733 T C 23 GENIC homozygous 791940488 19 56011013 56011014 C T 20 GENIC homozygous 791940489 19 56011203 56011204 C T 35 GENIC homozygous 791940490 19 56011543 56011544 T C 37 GENIC homozygous 791940491 19 56011979 56011980 C T 17 GENIC homozygous 791940492 19 56012029 56012030 G A 12 GENIC homozygous 791940493 19 56012468 56012469 C A 39 GENIC homozygous 791940494 19 56012835 56012836 T C 22 GENIC homozygous 791940495 19 56014649 56014650 C G 13 GENIC homozygous 791940496 19 56014664 56014665 A G 11 GENIC homozygous 791940497 19 56014888 56014889 A T 32 GENIC homozygous 791940498 19 56015842 56015843 G A 3 GENIC homozygous 791940499 19 56016113 56016114 C A 26 GENIC homozygous 791940500 19 56016700 56016701 G A 31 GENIC heterozygous 791940501 19 56016888 56016889 G A 22 GENIC homozygous 791940502 19 56017375 56017376 C T 18 GENIC heterozygous 791940503 19 56017436 56017437 T A 16 GENIC homozygous 791940504 19 56017846 56017847 T A 18 GENIC homozygous 791940505 19 56017905 56017906 T C 18 GENIC homozygous 791940506 19 56018570 56018571 G A 33 GENIC homozygous 791940507 19 56018948 56018949 G A 14 GENIC possibly homozygous 791940508 19 56019292 56019293 T C 22 GENIC homozygous 791940509 19 56019695 56019696 C T 23 GENIC homozygous 791940510 19 56019753 56019754 A G 24 GENIC homozygous 791940511 19 56019944 56019945 C T 19 GENIC homozygous 791940512 19 56020046 56020047 G T 16 GENIC possibly homozygous 791940513 19 56020331 56020332 G A 23 GENIC homozygous 791940514 19 56020497 56020498 T C 32 GENIC homozygous 791940515 19 56021246 56021247 T C 13 GENIC heterozygous 791940516 19 56021265 56021266 T C 11 GENIC homozygous 791940517