chr start stop reference nuc variant nuc depth genic status zygosity variant ID 13 90809919 90809920 A T 31 GENIC homozygous 939163006 13 90810724 90810725 G A 22 GENIC homozygous 939163007 13 90811630 90811631 A G 26 GENIC homozygous 939163008 13 90813470 90813471 A G 9 GENIC homozygous 939163009 13 90814817 90814818 A G 24 GENIC homozygous 939163010 13 90815585 90815586 T A 11 GENIC homozygous 939163011 13 90815764 90815765 C T 12 GENIC homozygous 939163012 13 90816550 90816551 A G 24 GENIC homozygous 939163013 13 90819680 90819681 C T 20 GENIC homozygous 939163014 13 90821272 90821273 G A 30 GENIC homozygous 939163015 13 90824055 90824056 C T 14 GENIC homozygous 939163016 13 90824674 90824675 G A 23 GENIC homozygous 939163017 13 90825257 90825258 T A 27 GENIC homozygous 939163018 13 90825273 90825274 A G 25 GENIC homozygous 939163019 13 90825566 90825567 C T 24 GENIC homozygous 939163020 13 90825670 90825671 G A 29 GENIC homozygous 939163021 13 90825887 90825888 G A 22 GENIC homozygous 939163022 13 90826025 90826026 T C 22 GENIC homozygous 939163023 13 90826659 90826660 A G 22 GENIC homozygous 939163024 13 90829066 90829067 A G 13 GENIC homozygous 939163025