chr start stop reference nuc variant nuc depth genic status zygosity variant ID X 62841206 62841207 G A 27 GENIC homozygous 108382386 X 62858220 62858220 TGTGATTC 19 GENIC homozygous 129748626 X 62873046 62873047 C A 25 GENIC homozygous 108268137 X 62873052 62873053 T C 25 GENIC homozygous 108268139 X 62873073 62873074 A 25 GENIC homozygous 129748631 X 62873089 62873090 T C 27 GENIC homozygous 108268141 X 62879865 62879866 A G 22 GENIC homozygous 108447067 X 62879869 62879870 A G 21 GENIC homozygous 108447069 X 62891525 62891526 C 13 GENIC homozygous 129748637 X 62891532 62891534 TC 13 GENIC homozygous 129748638 X 62897856 62897857 C 35 GENIC homozygous 129748639 X 62895406 62895407 G A 14 GENIC homozygous 108644827