chr start stop reference nuc variant nuc depth genic status zygosity variant ID 10 110139141 110139142 A - 12 GENIC homozygous 52684191 10 110139153 110139154 A G 20 GENIC homozygous 52814776 10 110139500 110139501 C T 32 GENIC homozygous 51601059 10 110140004 110140007 AAA --- 15 GENIC possibly homozygous 51601060 10 110140154 110140155 A G 40 GENIC homozygous 51601062 10 110140346 110140347 A - 14 GENIC homozygous 51601063 10 110140426 110140427 A AGG 1 GENIC homozygous 52814779 10 110140635 110140636 A G 18 GENIC homozygous 51601064 10 110140738 110140739 G A 16 GENIC homozygous 51601065 10 110140784 110140785 G T 14 GENIC homozygous 51601066 10 110142723 110142725 AA -- 25 INTERGENIC homozygous 51601067 10 110142859 110142860 T C 28 INTERGENIC homozygous 51601068 10 110145666 110145667 T C 24 GENIC homozygous 51601069 10 110146190 110146191 A G 30 GENIC homozygous 51601070 10 110147331 110147332 G A 30 GENIC homozygous 51601073 10 110147657 110147658 C A 31 GENIC homozygous 51601074 10 110147827 110147828 A C 41 GENIC homozygous 51601075