chr start stop reference nuc variant nuc depth genic status zygosity variant ID 3 159995368 159995370 AG 11 GENIC homozygous 127948141 3 159996063 159996064 T C 20 GENIC homozygous 111791119 3 159996198 159996199 A G 19 GENIC homozygous 111791121 3 159996625 159996626 A G 18 GENIC homozygous 111791123 3 159996640 159996641 C T 20 GENIC possibly homozygous 111791125 3 159996681 159996682 G A 20 GENIC homozygous 111791127 3 159997704 159997704 T 11 GENIC homozygous 127948142 3 159998011 159998012 A G 20 GENIC homozygous 111791129 3 159998102 159998103 A G 24 GENIC homozygous 111791131 3 160000272 160000273 G A 15 GENIC homozygous 111791133 3 160002606 160002607 C 4 GENIC homozygous 127948143 3 160005018 160005019 C T 12 GENIC homozygous 111791135 3 160008150 160008151 C G 12 GENIC homozygous 111791137 3 160009225 160009226 C T 17 GENIC homozygous 111791138 3 160010164 160010165 A G 17 GENIC homozygous 111791140 3 160010762 160010763 G C 16 GENIC homozygous 111791142 3 160011071 160011074 GTG 23 GENIC homozygous 127948144 3 160011322 160011323 C A 19 GENIC homozygous 111791144 3 160011765 160011766 A G 23 GENIC homozygous 111791146 3 160013805 160013806 A G 19 GENIC homozygous 111791148 3 160014125 160014126 A T 20 GENIC homozygous 111791150 3 160014630 160014631 G A 26 GENIC homozygous 111791152