chr start stop reference nuc variant nuc depth genic status zygosity variant ID 10 69434988 69434989 C 19 GENIC possibly homozygous 128828381 10 69435289 69435290 C G 15 GENIC homozygous 116625112 10 69435303 69435304 C G 15 GENIC homozygous 116625114 10 69436518 69436519 G A 10 GENIC homozygous 116625116 10 69436690 69436691 T G 15 GENIC homozygous 116625118 10 69436817 69436818 T A 15 GENIC homozygous 116625120 10 69437128 69437129 G C 9 GENIC homozygous 116625122 10 69437779 69437780 A G 16 GENIC homozygous 116625124 10 69438203 69438204 A G 15 GENIC homozygous 116625126 10 69438668 69438669 A C 9 GENIC homozygous 116625128 10 69438669 69438670 T C 9 GENIC homozygous 116625130 10 69438826 69438827 T G 12 GENIC homozygous 116625132 10 69439167 69439168 A T 14 GENIC homozygous 116625134 10 69439212 69439213 T G 17 GENIC homozygous 116625136 10 69439232 69439233 A G 18 GENIC homozygous 116625138 10 69439272 69439273 T C 19 GENIC homozygous 116625140 10 69439325 69439326 T G 14 GENIC homozygous 116625142 10 69439520 69439521 G A 19 GENIC homozygous 116625144