chr start stop reference nuc variant nuc depth genic status zygosity variant ID 5 156466955 156466956 T C 38 GENIC homozygous 508755374 5 156467036 156467037 C T 46 GENIC homozygous 506518727 5 156467062 156467063 A G 53 GENIC homozygous 506518728 5 156468021 156468022 G C 49 GENIC homozygous 508755375 5 156468097 156468100 TCT --- 40 GENIC homozygous 685715476 5 156468792 156468793 A - 60 GENIC homozygous 685715477 5 156469168 156469169 G A 59 GENIC homozygous 506518729 5 156469329 156469330 A G 69 GENIC homozygous 506518730 5 156469343 156469344 G T 59 GENIC homozygous 506518731 5 156469557 156469558 A C 56 GENIC homozygous 506518732 5 156469704 156469705 A G 44 GENIC homozygous 506518733 5 156469734 156469735 A G 47 GENIC homozygous 506518734 5 156469760 156469761 A G 58 GENIC possibly homozygous 506518735 5 156469885 156469886 A ATT 2 GENIC heterozygous 685715479 5 156469886 156469887 T - 2 GENIC heterozygous 685715478 5 156470006 156470007 A G 44 GENIC homozygous 506518736 5 156470324 156470325 A G 36 GENIC homozygous 506518737 5 156470972 156470973 G A 60 GENIC possibly homozygous 506518738 5 156471550 156471551 G A 60 GENIC homozygous 506518739 5 156472254 156472255 A G 99 GENIC heterozygous 508755376