chr start stop reference nuc variant nuc depth genic status zygosity variant ID 10 66133377 66133378 C - 19 GENIC homozygous 51907758 10 66134758 66134759 C CTCTG 16 GENIC homozygous 51479126 10 66134759 66134760 A G 16 GENIC homozygous 52382562 10 66136919 66136993 CACCCCCACCCCACCCCACTTGACCAGGCAGTCCTGCTTATTTTCAGGCCCCCAGCTTTCACGTGGTGTACAGG -------------------------------------------------------------------------- 1 GENIC homozygous 52382564 10 66137130 66137131 T - 7 GENIC homozygous 52382566 10 66140930 66140931 C G 15 GENIC homozygous 51479147 10 66140931 66140932 C A 15 GENIC homozygous 51479148 10 66140939 66140940 G T 16 GENIC homozygous 51479149 10 66140941 66140942 A - 16 GENIC homozygous 51479150 10 66140944 66140945 T C 16 GENIC homozygous 52382568 10 66140945 66140946 A T 16 GENIC homozygous 52382570 10 66140958 66140959 G C 15 GENIC homozygous 51479151 10 66140960 66140961 G T 15 GENIC homozygous 51479152 10 66140963 66140964 G T 14 GENIC homozygous 51479153 10 66140966 66140967 T - 14 GENIC homozygous 51479154 10 66140985 66140986 A T 11 GENIC homozygous 51479155 10 66140987 66140988 G A 11 GENIC homozygous 51479156 10 66140990 66140991 A - 10 GENIC homozygous 51479157 10 66141000 66141001 A - 8 GENIC homozygous 51479158 10 66141014 66141015 A - 8 GENIC homozygous 51479159 10 66141028 66141029 A - 7 GENIC homozygous 51479160 10 66141052 66141054 TG -- 3 GENIC homozygous 51479164 10 66141089 66141090 A - 1 GENIC homozygous 51479168 10 66141109 66141110 C CA 3 GENIC homozygous 51479169 10 66141192 66141199 CCCAGCC ------- 15 GENIC homozygous 51479170 10 66141506 66141507 G GAA 14 GENIC heterozygous 51479171 10 66141506 66141507 G GA 14 GENIC heterozygous 51678674 10 66147045 66147046 G - 11 GENIC homozygous 51479181 10 66150710 66150711 C CA 7 GENIC heterozygous 51479188 10 66156768 66156769 A G 24 GENIC homozygous 51479193 10 66162694 66162695 A - 2 GENIC homozygous 51678676