chr start stop reference nuc variant nuc depth genic status zygosity variant ID 19 57342970 57342971 T C 18 GENIC homozygous 998988045 19 57347480 57347481 A T 10 GENIC homozygous 998988046 19 57357077 57357078 C A 18 GENIC homozygous 998988047 19 57357754 57357755 A G 23 GENIC homozygous 998988048 19 57360676 57360677 G C 29 GENIC homozygous 998988049 19 57362898 57362899 A G 15 GENIC homozygous 998988050 19 57368153 57368154 C A 35 GENIC homozygous 998988051 19 57368526 57368527 G A 20 GENIC homozygous 998988052 19 57375861 57375862 T C 28 GENIC homozygous 998988053 19 57375887 57375888 C G 27 GENIC homozygous 998988054 19 57376014 57376015 A T 20 GENIC homozygous 998988055 19 57376471 57376472 A G 28 GENIC homozygous 998988056 19 57376493 57376494 C T 26 GENIC homozygous 998988057 19 57376661 57376662 G A 26 GENIC homozygous 998988058 19 57377402 57377403 C A 18 GENIC homozygous 998988059 19 57377436 57377437 A G 21 GENIC possibly homozygous 998988060 19 57377836 57377837 T C 15 GENIC homozygous 998988061 19 57377928 57377929 T C 25 GENIC homozygous 998988062 19 57378075 57378076 T C 37 GENIC homozygous 998988063 19 57378437 57378438 A G 15 GENIC homozygous 998988064