chr start stop reference nuc variant nuc depth genic status zygosity variant ID 7 123006322 123006323 A G 19 GENIC homozygous 54088929 7 123006866 123006867 C T 14 GENIC homozygous 54088932 7 123007096 123007097 C CTT 3 GENIC homozygous 54088933 7 123007445 123007447 AC -- 6 GENIC heterozygous 56171581 7 123007581 123007582 A - 27 GENIC homozygous 54088934 7 123008012 123008013 A AATAT 1 GENIC homozygous 55280423 7 123008068 123008069 A G 3 GENIC heterozygous 54088940 7 123008210 123008211 G A 6 GENIC homozygous 54088941 7 123008288 123008289 A G 23 GENIC heterozygous 54088942 7 123008851 123008852 C - 16 GENIC homozygous 54088943 7 123010551 123010552 G A 14 GENIC homozygous 56171583 7 123011831 123011832 A C 15 GENIC homozygous 54088944 7 123016222 123016223 A - 4 GENIC heterozygous 54088948 7 123016993 123016994 C T 19 GENIC heterozygous 56171585 7 123020846 123020847 G A 26 GENIC possibly homozygous 54088950 7 123021593 123021594 G A 23 GENIC homozygous 54088951 7 123025959 123025960 G C 12 GENIC homozygous 54088952 7 123026879 123026880 T G 20 GENIC possibly homozygous 54088956 7 123027529 123027530 A G 12 GENIC homozygous 54088960 7 123033013 123033014 T C 18 GENIC heterozygous 54088961