chr start stop reference nuc variant nuc depth genic status zygosity variant ID 3 83029720 83029721 C 19 GENIC heterozygous 129890269 3 83037581 83037582 G 42 GENIC homozygous 127902097 3 83037608 83037608 A 31 GENIC homozygous 127902098 3 83037623 83037624 C 32 GENIC homozygous 127902099 3 83037636 83037636 C 28 GENIC homozygous 127902100 3 83037650 83037650 T 29 GENIC homozygous 127902101 3 83037657 83037657 C 28 GENIC homozygous 127902102 3 83037680 83037681 G 24 GENIC homozygous 127902103 3 83037686 83037687 A 29 GENIC homozygous 127902104 3 83037702 83037703 A 32 GENIC homozygous 127902105 3 83037726 83037727 G 34 GENIC homozygous 127902106 3 83037782 83037783 G A 41 GENIC homozygous 111953266 3 83037783 83037784 A C 42 GENIC homozygous 111953268 3 83037796 83037796 T 38 GENIC homozygous 127902107 3 83037867 83037868 T 37 GENIC homozygous 127902108 3 83037873 83037873 T 36 GENIC homozygous 127902109 3 83037909 83037910 G 36 GENIC homozygous 127902110 3 83037918 83037919 G 34 GENIC homozygous 127902111 3 83037977 83037977 GGG 26 GENIC homozygous 127902112 3 83037988 83037988 A 26 GENIC homozygous 127902113 3 83037989 83037990 A G 27 GENIC homozygous 119650410 3 83037997 83037997 G 26 GENIC homozygous 127902114 3 83038049 83038049 C 31 GENIC homozygous 127902115 3 83038052 83038053 G T 31 GENIC homozygous 119650411 3 83038056 83038057 T 30 GENIC homozygous 127902116 3 83038063 83038064 G 33 GENIC homozygous 127902117 3 83038071 83038073 CA 38 GENIC homozygous 127902118 3 83038075 83038075 TCT 38 GENIC homozygous 127902119