chr start stop reference nuc variant nuc depth genic status zygosity variant ID 10 105074742 105074743 A G 3 GENIC heterozygous 118012454 10 105074759 105074760 A G 7 GENIC possibly homozygous 118012455 10 105074776 105074777 A G 13 GENIC homozygous 118012456 10 105074813 105074814 C G 23 GENIC homozygous 117145104 10 105074815 105074816 A G 23 GENIC homozygous 117031602 10 105075001 105075002 A G 56 GENIC homozygous 116713770 10 105075005 105075006 A G 53 GENIC homozygous 116713772 10 105075007 105075008 A T 53 GENIC homozygous 116713774 10 105075019 105075020 A G 48 GENIC homozygous 116713776 10 105075022 105075023 C G 45 GENIC homozygous 116713778 10 105075031 105075032 A G 44 GENIC homozygous 116961680 10 105075035 105075036 A G 44 GENIC possibly homozygous 116713780 10 105075037 105075038 G T 44 GENIC possibly homozygous 116713782 10 105075081 105075082 A G 49 GENIC homozygous 116713784 10 105081148 105081149 C T 37 GENIC heterozygous 118012458 10 105083233 105083234 C T 16 GENIC heterozygous 118012461 10 105083300 105083301 C T 60 GENIC heterozygous 118012462 10 105094984 105094985 G A 43 GENIC homozygous 116713790 10 105086229 105086230 A G 28 GENIC heterozygous 118126520