chr start stop reference nuc variant nuc depth genic status zygosity variant ID 6 115045146 115045147 T TTTCCA 32 GENIC possibly homozygous 54657025 6 115046105 115046106 A G 24 GENIC homozygous 54657027 6 115046469 115046470 A C 24 GENIC homozygous 54657029 6 115046730 115046731 T TACCAATGCCTTCCTTCATA 20 GENIC homozygous 55531482 6 115046833 115046834 T C 20 GENIC homozygous 54657035 6 115046835 115046836 T A 21 GENIC homozygous 54657037 6 115047003 115047005 TT -- 17 GENIC homozygous 54657039 6 115047396 115047397 C T 18 GENIC homozygous 54657041 6 115048071 115048072 A G 21 GENIC homozygous 54657043 6 115048337 115048338 A C 35 GENIC possibly homozygous 54657045 6 115048749 115048750 A T 20 GENIC homozygous 54657047 6 115053567 115053573 GTGTGT ------ 6 GENIC homozygous 55975920 6 115054494 115054495 C - 15 GENIC homozygous 54657049 6 115054868 115054870 TT -- 2 GENIC heterozygous 55427606 6 115056182 115056183 G A 22 GENIC possibly homozygous 54657056