chr start stop reference nuc variant nuc depth genic status zygosity variant ID 10 82047976 82047977 C A 19 GENIC homozygous 116812518 10 82076602 82076603 C T 15 GENIC homozygous 116812524 10 82077438 82077439 A G 19 GENIC homozygous 116658038 10 82078382 82078383 T C 30 GENIC homozygous 116658040 10 82081147 82081148 T C 20 GENIC homozygous 116658050 10 82089285 82089286 T C 20 GENIC homozygous 116658062 10 82094159 82094160 G A 25 GENIC homozygous 116658068 10 82090570 82090571 A T 28 GENIC homozygous 116658064 10 82092332 82092333 C T 14 GENIC homozygous 116812528 10 82093866 82093867 T A 17 GENIC homozygous 116658066 10 82094181 82094182 G A 21 GENIC homozygous 116658070 10 82094744 82094745 T C 22 GENIC homozygous 116658072 10 82095828 82095829 G A 24 GENIC homozygous 116658074 10 82096072 82096073 T A 20 GENIC homozygous 116812530 10 82096385 82096386 C T 27 GENIC homozygous 116812532 10 82103253 82103254 T C 17 GENIC homozygous 116658076 10 82106797 82106798 C A 25 GENIC homozygous 116658078 10 82106879 82106880 T G 18 GENIC homozygous 116658080 10 82108722 82108723 G A 24 GENIC homozygous 116812534 10 82109430 82109431 T C 14 GENIC homozygous 116658084 10 82114466 82114467 T C 29 GENIC homozygous 116658086