chr start stop reference nuc variant nuc depth genic status zygosity variant ID 5 59490763 59490764 A G 25 GENIC homozygous 957957946 5 59491034 59491035 G A 18 GENIC homozygous 957957947 5 59491087 59491088 A C 16 GENIC heterozygous 957957948 5 59492252 59492253 G A 31 GENIC homozygous 957957949 5 59493293 59493294 T C 28 GENIC homozygous 957957950 5 59493344 59493345 C T 23 GENIC homozygous 957957951 5 59494021 59494022 G T 23 GENIC homozygous 957957952 5 59495021 59495022 A G 21 GENIC homozygous 957957953 5 59496242 59496243 A G 24 GENIC homozygous 957957954 5 59497270 59497271 G A 30 GENIC homozygous 957957955 5 59500179 59500180 A G 21 GENIC homozygous 957957956 5 59500828 59500829 G C 26 GENIC homozygous 957957957 5 59500873 59500874 G A 28 GENIC homozygous 957957958 5 59500875 59500876 C T 28 GENIC homozygous 957957959 5 59502207 59502208 C A 20 GENIC homozygous 957957960 5 59502243 59502244 C T 20 GENIC homozygous 957957961 5 59502300 59502301 G A 19 GENIC homozygous 957957962 5 59502340 59502341 C T 18 GENIC homozygous 957957963 5 59502468 59502469 C T 23 GENIC homozygous 957957964 5 59502683 59502684 T C 24 GENIC homozygous 957957965 5 59502698 59502699 A T 23 GENIC homozygous 957957966 5 59503232 59503233 C T 24 GENIC homozygous 957957967 5 59503245 59503246 C T 30 GENIC homozygous 957957968 5 59503453 59503454 C T 32 GENIC homozygous 957957969 5 59503514 59503515 T C 20 GENIC homozygous 957957970 5 59503720 59503721 T C 18 GENIC possibly homozygous 957957971 5 59504116 59504117 T C 9 GENIC homozygous 957957972 5 59504488 59504489 A G 23 GENIC homozygous 957957973 5 59504888 59504889 T C 21 GENIC homozygous 957957974 5 59505140 59505141 C T 29 GENIC homozygous 957957975 5 59505463 59505464 T C 23 GENIC homozygous 957957976 5 59505718 59505719 G A 26 GENIC homozygous 957957977