chr start stop reference nuc variant nuc depth genic status zygosity variant ID 5 92269075 92269076 G T 32 GENIC homozygous 519921593 5 92269612 92269613 C CG 50 GENIC homozygous 690687569 5 92269749 92269750 A G 39 GENIC homozygous 519921594 5 92269820 92269821 C T 47 GENIC possibly homozygous 519921595 5 92270563 92270564 G T 48 GENIC homozygous 519921596 5 92270583 92270588 TTCTG ----- 22 GENIC homozygous 690687570 5 92270723 92270724 T C 35 GENIC possibly homozygous 519921597 5 92271050 92271051 A G 42 GENIC homozygous 519921598 5 92271089 92271090 G A 46 GENIC possibly homozygous 519921599 5 92271322 92271323 T TA 26 GENIC homozygous 690687571 5 92272505 92272506 C T 45 GENIC homozygous 519921600 5 92272790 92272791 G T 60 GENIC possibly homozygous 519921601 5 92272838 92272839 G T 50 GENIC homozygous 519921602 5 92272913 92272914 A G 40 GENIC homozygous 519921603 5 92273832 92273833 T C 40 GENIC possibly homozygous 522088157 5 92274188 92274189 C T 40 GENIC homozygous 522088158 5 92274598 92274599 G A 53 GENIC homozygous 522088159 5 92274645 92274646 A C 42 GENIC possibly homozygous 522088160 5 92274922 92274923 A G 50 GENIC homozygous 522088161 5 92275069 92275070 G A 41 GENIC homozygous 522088162 5 92275227 92275228 C T 44 GENIC homozygous 522088163 5 92275714 92275715 T G 55 GENIC homozygous 519921604 5 92276027 92276028 G A 28 GENIC homozygous 519921605 5 92276604 92276605 C G 41 GENIC homozygous 519921606