chr start stop reference nuc variant nuc depth genic status zygosity variant ID 8 53660904 53660905 C T 19 GENIC homozygous 52634285 8 53661778 53661779 G GA 16 GENIC homozygous 52634287 8 53662308 53662309 G C 18 GENIC homozygous 52634289 8 53662432 53662433 T A 23 GENIC homozygous 52634291 8 53662629 53662630 T C 13 GENIC possibly homozygous 52634293 8 53664035 53664036 A G 11 GENIC homozygous 52634301 8 53665181 53665182 T C 18 GENIC possibly homozygous 52634309 8 53665991 53665992 G GAAAAAGAC 4 GENIC heterozygous 53339980 8 53666742 53666743 G A 16 GENIC possibly homozygous 53339982 8 53670020 53670021 A C 7 GENIC heterozygous 52634313 8 53672125 53672126 G - 16 GENIC homozygous 53339984 8 53672241 53672242 G A 23 GENIC possibly homozygous 52634315 8 53674348 53674349 T A 18 GENIC homozygous 52634321 8 53677856 53677857 G GA 13 GENIC homozygous 53339986 8 53678592 53678593 A T 21 GENIC homozygous 52634329 8 53678891 53678892 G A 3 GENIC heterozygous 53339988 8 53681734 53681735 G A 12 GENIC possibly homozygous 53339990 8 53681879 53681880 C CTG 7 GENIC possibly homozygous 52634357 8 53681963 53681965 GT -- 6 GENIC homozygous 52634359 8 53682728 53682729 A G 23 GENIC possibly homozygous 53339992 8 53682888 53682889 C T 23 GENIC homozygous 53339994 8 53684113 53684114 T TA 8 GENIC homozygous 53339996