chr start stop reference nuc variant nuc depth genic status zygosity variant ID 4 114981309 114981310 G A 7 GENIC homozygous 119527006 4 114981762 114981763 C T 12 GENIC homozygous 119527008 4 114982011 114982012 A C 11 GENIC homozygous 112814018 4 114982113 114982114 A G 22 GENIC homozygous 112814020 4 114982630 114982631 A G 23 GENIC homozygous 112814026 4 114982749 114982750 T C 22 GENIC homozygous 112814028 4 114982789 114982790 A C 17 GENIC homozygous 119527010 4 114986427 114986428 G A 16 GENIC homozygous 112814044 4 114986604 114986605 C T 18 GENIC homozygous 112814046 4 114986648 114986649 C T 19 GENIC homozygous 112814052 4 114986711 114986712 G T 19 GENIC homozygous 119527012 4 114986932 114986933 G A 13 GENIC possibly homozygous 119527014 4 114987447 114987448 T C 17 GENIC homozygous 112814054 4 114987529 114987530 T G 15 GENIC homozygous 119527016 4 114987630 114987631 G A 17 GENIC homozygous 112814056 4 114987720 114987721 C T 17 GENIC homozygous 112814058 4 114987781 114987782 C T 12 GENIC possibly homozygous 112814060