chr start stop reference nuc variant nuc depth genic status zygosity variant ID 19 56010732 56010733 T C 26 GENIC homozygous 939765087 19 56011013 56011014 C T 18 GENIC homozygous 939765088 19 56011203 56011204 C T 18 GENIC homozygous 939765089 19 56011543 56011544 T C 14 GENIC homozygous 939765090 19 56011979 56011980 C T 23 GENIC homozygous 939765091 19 56012029 56012030 G A 19 GENIC homozygous 939765092 19 56012468 56012469 C A 24 GENIC homozygous 939765093 19 56012835 56012836 T C 31 GENIC homozygous 939765094 19 56014649 56014650 C G 18 GENIC homozygous 939765095 19 56014664 56014665 A G 17 GENIC homozygous 939765096 19 56014888 56014889 A T 22 GENIC homozygous 939765097 19 56016888 56016889 G A 12 GENIC homozygous 939765098 19 56017436 56017437 T A 16 GENIC homozygous 939765099 19 56017846 56017847 T A 19 GENIC homozygous 939765100 19 56017905 56017906 T C 27 GENIC homozygous 939765101 19 56018570 56018571 G A 24 GENIC homozygous 939765102 19 56019292 56019293 T C 15 GENIC homozygous 939765103 19 56019695 56019696 C T 13 GENIC homozygous 939765104 19 56019753 56019754 A G 22 GENIC homozygous 939765105 19 56019944 56019945 C T 22 GENIC homozygous 939765106 19 56020331 56020332 G A 26 GENIC homozygous 939765107 19 56020497 56020498 T C 18 GENIC homozygous 939765108