chr start stop reference nuc variant nuc depth genic status zygosity variant ID 3 125429054 125429055 T C 46 GENIC homozygous 112298029 3 125431067 125431068 T G 28 GENIC homozygous 112298031 3 125431172 125431173 C G 30 GENIC homozygous 111696114 3 125431267 125431268 A G 44 GENIC homozygous 112298033 3 125431424 125431425 T C 41 GENIC homozygous 112298035 3 125431914 125431915 A G 61 GENIC homozygous 112298037 3 125432160 125432161 T G 51 GENIC possibly homozygous 112298039 3 125432686 125432687 A T 44 GENIC homozygous 111696120 3 125434398 125434399 T A 34 GENIC homozygous 112298041 3 125434985 125434986 C T 35 GENIC homozygous 112298043 3 125435024 125435025 T C 33 GENIC homozygous 112298045 3 125435489 125435490 G A 52 GENIC possibly homozygous 112298047 3 125435673 125435674 A T 35 GENIC possibly homozygous 112298049 3 125435698 125435699 C T 20 GENIC homozygous 112298051 3 125439145 125439146 G A 40 GENIC homozygous 112298053 3 125439747 125439748 A G 37 GENIC homozygous 111696126 3 125440437 125440438 G A 37 GENIC homozygous 112298055 3 125441249 125441250 C T 30 GENIC homozygous 112298057 3 125441322 125441323 A G 31 GENIC homozygous 111696130