chr start stop reference nuc variant nuc depth genic status zygosity variant ID 17 41801055 41801056 G A 22 GENIC homozygous 936578869 17 41801228 41801229 T C 25 GENIC homozygous 936578870 17 41801899 41801900 G A 34 GENIC homozygous 936578871 17 41802420 41802421 G A 31 GENIC homozygous 936578872 17 41802895 41802896 T C 33 GENIC homozygous 936578873 17 41803064 41803065 G A 24 GENIC homozygous 936578874 17 41803331 41803332 A G 24 GENIC homozygous 936578875 17 41803723 41803724 A G 35 GENIC homozygous 936578876 17 41804579 41804580 C A 35 GENIC homozygous 936578877 17 41804691 41804692 A T 23 GENIC homozygous 936578878 17 41805049 41805050 A G 24 GENIC homozygous 936578879 17 41805653 41805654 G A 30 GENIC homozygous 936578880 17 41805760 41805761 T C 33 GENIC homozygous 936578881 17 41806052 41806053 G T 14 GENIC homozygous 936578882 17 41807132 41807133 C T 21 GENIC homozygous 936578883 17 41807849 41807850 T C 37 GENIC homozygous 936578884 17 41808996 41808997 A G 14 GENIC homozygous 936578885 17 41809399 41809400 C G 22 GENIC homozygous 936578886 17 41809606 41809607 C T 30 GENIC homozygous 936578887 17 41809607 41809608 T A 30 GENIC homozygous 936578888 17 41811273 41811274 T C 16 GENIC homozygous 936578889 17 41811480 41811481 G A 33 GENIC homozygous 936578890 17 41811519 41811520 T G 22 GENIC homozygous 936578891 17 41811800 41811801 T C 32 GENIC homozygous 936578892 17 41815347 41815348 A C 20 GENIC homozygous 936578893 17 41815395 41815396 G A 18 GENIC homozygous 936578894