chr start stop reference nuc variant nuc depth genic status zygosity variant ID 19 56010732 56010733 T C 34 GENIC homozygous 936790536 19 56011013 56011014 C T 32 GENIC homozygous 936790537 19 56011203 56011204 C T 25 GENIC homozygous 936790538 19 56011543 56011544 T C 7 GENIC homozygous 936790539 19 56011979 56011980 C T 17 GENIC homozygous 936790540 19 56012029 56012030 G A 23 GENIC homozygous 936790541 19 56012468 56012469 C A 17 GENIC homozygous 936790542 19 56012835 56012836 T C 15 GENIC homozygous 936790543 19 56014649 56014650 C G 26 GENIC homozygous 936790544 19 56014664 56014665 A G 28 GENIC possibly homozygous 936790545 19 56014888 56014889 A T 25 GENIC homozygous 936790546 19 56016113 56016114 C A 17 GENIC homozygous 936790547 19 56016888 56016889 G A 28 GENIC homozygous 936790548 19 56017436 56017437 T A 27 GENIC homozygous 936790549 19 56017846 56017847 T A 22 GENIC homozygous 936790550 19 56017905 56017906 T C 28 GENIC homozygous 936790551 19 56018570 56018571 G A 27 GENIC homozygous 936790552 19 56019292 56019293 T C 19 GENIC homozygous 936790553 19 56019695 56019696 C T 25 GENIC homozygous 936790554 19 56019753 56019754 A G 28 GENIC homozygous 936790555 19 56019944 56019945 C T 16 GENIC homozygous 936790556 19 56020331 56020332 G A 22 GENIC homozygous 936790557 19 56020497 56020498 T C 23 GENIC possibly homozygous 936790558 19 56021385 56021386 C A 22 GENIC homozygous 936790559