chr start stop reference nuc variant nuc depth genic status zygosity variant ID 19 56010732 56010733 T C 65 GENIC homozygous 810060433 19 56011013 56011014 C T 45 GENIC homozygous 810060434 19 56011203 56011204 C T 55 GENIC homozygous 810060435 19 56011543 56011544 T C 48 GENIC homozygous 810060436 19 56011979 56011980 C T 52 GENIC possibly homozygous 810060437 19 56012029 56012030 G A 41 GENIC homozygous 810060438 19 56012468 56012469 C A 74 GENIC possibly homozygous 810060439 19 56012835 56012836 T C 46 GENIC homozygous 810060440 19 56014649 56014650 C G 43 GENIC homozygous 810060441 19 56014664 56014665 A G 47 GENIC homozygous 810060442 19 56014888 56014889 A T 57 GENIC homozygous 810060443 19 56015842 56015843 G A 14 GENIC homozygous 810060444 19 56016113 56016114 C A 48 GENIC possibly homozygous 810060445 19 56016700 56016701 G A 59 GENIC heterozygous 810060446 19 56016888 56016889 G A 68 GENIC homozygous 810060447 19 56017375 56017376 C T 31 GENIC possibly homozygous 810060448 19 56017436 56017437 T A 36 GENIC homozygous 810060449 19 56017846 56017847 T A 41 GENIC homozygous 810060450 19 56017905 56017906 T C 40 GENIC possibly homozygous 810060451 19 56018570 56018571 G A 57 GENIC homozygous 810060452 19 56019292 56019293 T C 43 GENIC possibly homozygous 810060453 19 56019695 56019696 C T 42 GENIC homozygous 810060454 19 56019753 56019754 A G 35 GENIC homozygous 810060455 19 56019944 56019945 C T 30 GENIC homozygous 810060456 19 56020046 56020047 G T 33 GENIC possibly homozygous 810060457 19 56020331 56020332 G A 40 GENIC homozygous 810060458 19 56020497 56020498 T C 51 GENIC homozygous 810060459 19 56021246 56021247 T C 18 GENIC heterozygous 810060460 19 56021265 56021266 T C 19 GENIC homozygous 810060461