chr start stop reference nuc variant nuc depth genic status zygosity variant ID 5 92269075 92269076 G T 5 GENIC homozygous 524245246 5 92269612 92269613 C CG 9 GENIC homozygous 692339080 5 92269749 92269750 A G 8 GENIC homozygous 524245247 5 92269820 92269821 C T 19 GENIC homozygous 524245248 5 92270563 92270564 G T 7 GENIC homozygous 524245249 5 92270583 92270588 TTCTG ----- 6 GENIC heterozygous 692339081 5 92270723 92270724 T C 19 GENIC homozygous 524245250 5 92271050 92271051 A G 7 GENIC homozygous 524245251 5 92271089 92271090 G A 9 GENIC homozygous 524245252 5 92271322 92271323 T TA 9 GENIC homozygous 692339082 5 92272505 92272506 C T 24 GENIC possibly homozygous 524245253 5 92272790 92272791 G T 22 GENIC possibly homozygous 524245254 5 92272838 92272839 G T 19 GENIC homozygous 524245255 5 92272913 92272914 A G 20 GENIC homozygous 524245256 5 92273832 92273833 T C 18 GENIC homozygous 526377960 5 92274188 92274189 C T 18 GENIC homozygous 526377961 5 92274598 92274599 G A 24 GENIC homozygous 526377962 5 92274645 92274646 A C 23 GENIC homozygous 526377963 5 92274922 92274923 A G 16 GENIC homozygous 526377964 5 92275069 92275070 G A 21 GENIC possibly homozygous 526377965 5 92275227 92275228 C T 21 GENIC possibly homozygous 526377966 5 92275714 92275715 T G 13 GENIC homozygous 524245257 5 92276027 92276028 G A 7 GENIC homozygous 524245258 5 92276604 92276605 C G 21 GENIC homozygous 524245259