chr start stop reference nuc variant nuc depth genic status zygosity variant ID 12 40695537 40695538 A G 5 GENIC homozygous 994764622 12 40696133 40696134 C A 44 GENIC heterozygous 994764623 12 40696151 40696152 G A 40 GENIC homozygous 994764624 12 40696216 40696217 T C 35 GENIC homozygous 994764625 12 40696648 40696649 A T 22 GENIC homozygous 994764626 12 40696884 40696885 A T 15 GENIC homozygous 994764627 12 40697446 40697447 T C 13 GENIC homozygous 994764628 12 40697467 40697468 C T 17 GENIC homozygous 994764629 12 40698018 40698019 T G 4 GENIC homozygous 994764630 12 40698935 40698936 A G 17 GENIC homozygous 994764631 12 40702959 40702960 T C 27 GENIC homozygous 994764632 12 40705325 40705326 A G 24 GENIC homozygous 994764633 12 40707476 40707477 C T 26 GENIC homozygous 994764634 12 40709163 40709164 A G 31 GENIC homozygous 994764635