chr start stop reference nuc variant nuc depth genic status zygosity variant ID X 46978965 46978966 G T 5 GENIC homozygous 939874553 X 46978977 46978978 G A 5 GENIC homozygous 939874554 X 46978978 46978979 A G 5 GENIC homozygous 939874555 X 47004354 47004355 C T 10 GENIC homozygous 939874556 X 47008425 47008426 G A 11 GENIC homozygous 939874557 X 47008739 47008740 G A 6 GENIC homozygous 939874558 X 47009839 47009840 A G 16 GENIC homozygous 939874559 X 47011466 47011467 A G 11 GENIC homozygous 939874560 X 47011814 47011815 C T 14 GENIC homozygous 939874561 X 47013027 47013028 C T 13 GENIC homozygous 939874562 X 47014863 47014864 A C 15 GENIC homozygous 939874563 X 47016608 47016609 A G 6 GENIC homozygous 939874564 X 47020297 47020298 T C 5 GENIC homozygous 939874565 X 47025219 47025220 C T 11 GENIC homozygous 939874566 X 47025892 47025893 T C 12 GENIC homozygous 939874567