chr start stop reference nuc variant nuc depth genic status zygosity variant ID 20 14176930 14176930 T 11 GENIC homozygous 129662154 20 14176932 14176933 A 12 GENIC homozygous 129662155 20 14178043 14178044 G A 16 GENIC homozygous 109394314 20 14178096 14178096 C 21 GENIC homozygous 129662156 20 14178104 14178104 C 24 GENIC homozygous 129662157 20 14178135 14178136 T C 31 GENIC homozygous 119771297 20 14178194 14178195 A 36 GENIC homozygous 129662158 20 14178268 14178268 T 39 GENIC homozygous 129662159 20 14178280 14178280 CG 33 GENIC homozygous 129662160 20 14178575 14178576 A 8 GENIC homozygous 129662161 20 14178595 14178595 C 7 GENIC homozygous 129662162 20 14178632 14178633 C 29 GENIC homozygous 129662163 20 14178661 14178661 G 27 GENIC homozygous 129662164 20 14178676 14178676 G 29 GENIC homozygous 129662165 20 14178693 14178693 G 33 GENIC homozygous 129662166 20 14178719 14178719 C 33 GENIC homozygous 129662167 20 14178726 14178726 G 31 GENIC homozygous 129662168 20 14178734 14178734 A 30 GENIC homozygous 129662169 20 14178736 14178736 A 30 GENIC homozygous 129662170 20 14188634 14188635 T C 79 GENIC heterozygous 109101033 20 14188693 14188694 G C 81 GENIC heterozygous 109101035 20 14189333 14189334 G 76 GENIC heterozygous 129662182 20 14189334 14189335 C T 76 GENIC heterozygous 109101041 20 14189379 14189380 G C 60 GENIC heterozygous 109101043