chr start stop reference nuc variant nuc depth genic status zygosity variant ID 1 146752952 146752953 T 19 GENIC homozygous 127442835 1 146752958 146752958 T 20 GENIC homozygous 127442836 1 146752965 146752965 A 19 GENIC homozygous 127442837 1 146753018 146753019 A 14 GENIC homozygous 127442838 1 146753041 146753042 C 15 GENIC homozygous 127442839 1 146753058 146753059 G 16 GENIC homozygous 127442840 1 146753063 146753066 GGC 14 GENIC homozygous 127442841 1 146753068 146753069 C 13 GENIC homozygous 127442842 1 146753071 146753072 G C 13 GENIC homozygous 108278036 1 146753080 146753082 TA 15 GENIC homozygous 127442843 1 146753082 146753083 A C 15 GENIC homozygous 120486617 1 146778767 146778768 C 24 GENIC homozygous 127442860 1 146778800 146778800 T 23 GENIC homozygous 127442861 1 146778803 146778804 T 23 GENIC homozygous 127442862 1 146778848 146778849 C 18 GENIC homozygous 127442863 1 146787132 146787138 TGTTTA 9 GENIC homozygous 127442865 1 146787146 146787147 G 8 GENIC homozygous 127442866 1 146787150 146787154 AAAG 8 GENIC homozygous 127442867 1 146787156 146787156 T 8 GENIC homozygous 127442868 1 146787174 146787179 TAATT 4 GENIC homozygous 127442869 1 146796844 146796844 A 17 GENIC homozygous 127442872 1 146819938 146819940 AC 12 GENIC heterozygous 130620250 1 146787140 146787141 T A 8 GENIC homozygous 120473951