chr start stop reference nuc variant nuc depth genic status zygosity variant ID 7 104500582 104500583 G A 8 GENIC homozygous 115798536 7 104502630 104502631 A G 27 GENIC homozygous 115798538 7 104502849 104502850 A C 22 GENIC homozygous 118257924 7 104502850 104502851 C A 22 GENIC homozygous 118257926 7 104503037 104503038 G C 25 GENIC homozygous 118331991 7 104503621 104503622 A G 24 GENIC homozygous 115798542 7 104505923 104505924 C A 26 GENIC homozygous 115798544 7 104506018 104506019 G T 32 GENIC homozygous 115798546 7 104506383 104506384 T C 35 GENIC homozygous 115798548 7 104506692 104506693 A T 27 GENIC homozygous 115798550 7 104507078 104507079 T C 30 GENIC homozygous 115798552 7 104507088 104507089 G A 32 GENIC homozygous 115798554 7 104507976 104507977 G A 36 GENIC homozygous 115798556 7 104508348 104508349 A G 27 GENIC homozygous 115798558 7 104508795 104508796 G A 30 GENIC homozygous 115798560 7 104510607 104510608 A G 25 GENIC homozygous 115798562