chr start stop reference nuc variant nuc depth genic status zygosity variant ID 10 12881044 12881045 A C 21 GENIC possibly homozygous 510550153 10 12882223 12882224 G A 70 GENIC homozygous 507546838 10 12882631 12882635 ATAT ---- 39 GENIC homozygous 686083529 10 12883428 12883432 AAAC ---- 10 GENIC homozygous 686083530 10 12885559 12885560 G T 59 GENIC homozygous 507546839 10 12885869 12885870 T C 60 GENIC homozygous 507546840 10 12886049 12886050 G A 42 GENIC homozygous 510550154 10 12886209 12886210 T G 52 GENIC homozygous 507546841 10 12886530 12886531 G A 34 GENIC possibly homozygous 507546842 10 12886531 12886532 G A 35 GENIC possibly homozygous 507546843 10 12886559 12886560 G A 36 GENIC possibly homozygous 507546844 10 12886590 12886591 C G 30 GENIC homozygous 507546845 10 12886825 12886826 A G 53 GENIC homozygous 507546846 10 12887055 12887056 G A 67 GENIC homozygous 507546847 10 12887709 12887710 C T 52 GENIC homozygous 507546848 10 12888210 12888211 T TACAC 11 GENIC homozygous 686083531 10 12889294 12889295 A C 66 GENIC homozygous 507546849 10 12889666 12889667 G C 52 GENIC homozygous 507546850 10 12889935 12889936 C G 64 GENIC homozygous 507546851 10 12889957 12889958 T C 69 GENIC homozygous 507546852 10 12890050 12890051 A G 53 GENIC homozygous 507546853 10 12891096 12891097 T C 49 GENIC homozygous 507546854