chr start stop reference nuc variant nuc depth genic status zygosity variant ID 13 90809919 90809920 A T 33 GENIC homozygous 967793714 13 90810724 90810725 G A 22 GENIC homozygous 967793715 13 90811630 90811631 A G 18 GENIC homozygous 967793716 13 90813470 90813471 A G 13 GENIC homozygous 967793717 13 90814817 90814818 A G 23 GENIC homozygous 967793718 13 90815585 90815586 T A 13 GENIC homozygous 967793719 13 90815764 90815765 C T 16 GENIC homozygous 967793720 13 90816550 90816551 A G 22 GENIC homozygous 967793721 13 90819680 90819681 C T 21 GENIC homozygous 967793722 13 90821272 90821273 G A 31 GENIC homozygous 967793723 13 90824055 90824056 C T 26 GENIC homozygous 967793724 13 90824674 90824675 G A 23 GENIC homozygous 967793725 13 90825257 90825258 T A 32 GENIC homozygous 967793726 13 90825273 90825274 A G 27 GENIC homozygous 967793727 13 90825566 90825567 C T 14 GENIC homozygous 967793728 13 90825670 90825671 G A 13 GENIC homozygous 967793729 13 90825887 90825888 G A 36 GENIC homozygous 967793730 13 90826025 90826026 T C 28 GENIC homozygous 967793731 13 90826659 90826660 A G 21 GENIC homozygous 967793732 13 90829066 90829067 A G 39 GENIC homozygous 967793733