chr start stop reference nuc variant nuc depth genic status zygosity variant ID 5 134197078 134197079 C T 23 GENIC homozygous 975770031 5 134197761 134197762 T A 29 GENIC homozygous 975770032 5 134199531 134199532 T G 27 GENIC homozygous 975770033 5 134201404 134201405 G A 14 GENIC homozygous 975770034 5 134203699 134203700 C T 29 GENIC homozygous 975770035 5 134206183 134206184 A T 41 GENIC heterozygous 975770036 5 134206188 134206189 C T 42 GENIC heterozygous 975770037 5 134206205 134206206 G C 47 GENIC heterozygous 975770038 5 134206206 134206207 G C 47 GENIC heterozygous 975770039 5 134206221 134206222 G A 49 GENIC heterozygous 975770040 5 134206223 134206224 A G 52 GENIC heterozygous 975770041 5 134206283 134206284 T G 38 GENIC heterozygous 975770042 5 134206351 134206352 A G 39 GENIC heterozygous 975770043 5 134206406 134206407 T G 56 GENIC heterozygous 975770044 5 134206440 134206441 G T 63 GENIC heterozygous 975770045 5 134206615 134206616 C T 44 GENIC heterozygous 975770046 5 134206617 134206618 G T 42 GENIC heterozygous 975770047 5 134206707 134206708 C T 57 GENIC heterozygous 975770048 5 134206744 134206745 A G 67 GENIC heterozygous 975770049 5 134206769 134206770 G A 73 GENIC heterozygous 975770050 5 134206790 134206791 A G 79 GENIC heterozygous 975770051