chr start stop reference nuc variant nuc depth genic status zygosity variant ID 10 60487877 60487878 A T 27 GENIC homozygous 653788861 10 60487878 60487879 A C 27 GENIC possibly homozygous 653788862 10 60487949 60487950 T G 32 GENIC homozygous 653788863 10 60487992 60487993 A G 35 GENIC homozygous 653788864 10 60487997 60487998 C A 32 GENIC homozygous 653788865 10 60488025 60488026 A T 28 GENIC homozygous 653788866 10 60488063 60488064 T A 30 GENIC homozygous 653788867 10 60488223 60488224 C T 33 GENIC homozygous 653788868 10 60488327 60488328 A G 37 GENIC homozygous 653788869 10 60488349 60488350 C T 42 GENIC homozygous 653788870 10 60488356 60488357 T C 41 GENIC homozygous 653788871 10 60488386 60488387 A T 37 GENIC homozygous 653788872 10 60488449 60488450 G A 28 GENIC homozygous 653788873 10 60488450 60488451 G A 29 GENIC homozygous 653788874 10 60488462 60488463 T C 26 GENIC homozygous 653788875 10 60488610 60488611 A G 32 GENIC homozygous 653788876