chr start stop reference nuc variant nuc depth genic status zygosity variant ID 5 76182206 76182207 A G 25 GENIC homozygous 775317980 5 76182585 76182586 C A 32 GENIC homozygous 775317981 5 76182876 76182877 G A 41 GENIC possibly homozygous 775317982 5 76183331 76183332 A G 40 GENIC homozygous 775317983 5 76183382 76183383 T G 33 GENIC possibly homozygous 775317984 5 76183459 76183460 C G 37 GENIC homozygous 775317985 5 76184277 76184278 C A 58 GENIC heterozygous 775317986 5 76184775 76184776 G A 38 GENIC homozygous 775317987 5 76184798 76184799 A T 35 GENIC homozygous 775317988 5 76184837 76184838 T C 29 GENIC homozygous 775317989 5 76186217 76186218 G A 42 GENIC homozygous 775317990 5 76186447 76186448 G T 56 GENIC possibly homozygous 775317991 5 76186448 76186449 A T 55 GENIC homozygous 775317992 5 76186665 76186666 A G 30 GENIC homozygous 775317993 5 76187246 76187247 T C 26 GENIC homozygous 775317994