chr start stop reference nuc variant nuc depth genic status zygosity variant ID 10 82048165 82048166 A T 28 GENIC possibly homozygous 116658022 10 82062231 82062232 G T 22 GENIC homozygous 116812522 10 82070558 82070559 C T 25 GENIC homozygous 116658028 10 82071172 82071173 C T 35 GENIC homozygous 117172728 10 82075028 82075029 A G 17 GENIC homozygous 116658032 10 82077117 82077118 A G 32 GENIC possibly homozygous 116658034 10 82077389 82077390 T A 25 GENIC homozygous 116658036 10 82077438 82077439 A G 26 GENIC homozygous 116658038 10 82078382 82078383 T C 33 GENIC homozygous 116658040 10 82078703 82078704 G A 34 GENIC possibly homozygous 116658042 10 82079353 82079354 G C 22 GENIC possibly homozygous 116658044 10 82080791 82080792 T C 25 GENIC possibly homozygous 116658046 10 82081133 82081134 T C 23 GENIC possibly homozygous 116658048 10 82081147 82081148 T C 20 GENIC homozygous 116658050 10 82084866 82084867 T A 18 GENIC possibly homozygous 116658052 10 82086259 82086260 C T 33 GENIC homozygous 116658054 10 82086530 82086531 C T 28 GENIC homozygous 116658056 10 82088939 82088940 C T 43 GENIC homozygous 116658058 10 82088941 82088942 C A 43 GENIC homozygous 116658060 10 82089285 82089286 T C 17 GENIC homozygous 116658062 10 82090570 82090571 A T 24 GENIC homozygous 116658064 10 82091034 82091035 T C 26 GENIC homozygous 117370922 10 82093866 82093867 T A 20 GENIC homozygous 116658066 10 82094159 82094160 G A 16 GENIC homozygous 116658068 10 82094181 82094182 G A 15 GENIC homozygous 116658070 10 82094744 82094745 T C 34 GENIC homozygous 116658072 10 82095610 82095611 G A 10 GENIC heterozygous 116897986 10 82095828 82095829 G A 27 GENIC homozygous 116658074 10 82103253 82103254 T C 21 GENIC homozygous 116658076 10 82106797 82106798 C A 28 GENIC homozygous 116658078 10 82106879 82106880 T G 27 GENIC homozygous 116658080 10 82109430 82109431 T C 26 GENIC homozygous 116658084 10 82114466 82114467 T C 20 GENIC homozygous 116658086