chr start stop reference nuc variant nuc depth genic status zygosity variant ID 5 92269075 92269076 G T 4 GENIC homozygous 588991303 5 92269612 92269613 C CG 14 GENIC possibly homozygous 723936553 5 92269749 92269750 A G 8 GENIC homozygous 588991304 5 92269820 92269821 C T 11 GENIC possibly homozygous 588991305 5 92270563 92270564 G T 4 GENIC heterozygous 588991306 5 92270583 92270588 TTCTG ----- 1 GENIC homozygous 723936554 5 92270723 92270724 T C 4 GENIC homozygous 588991307 5 92271050 92271051 A G 12 GENIC possibly homozygous 588991308 5 92271089 92271090 G A 10 GENIC homozygous 588991309 5 92271322 92271323 T TA 5 GENIC heterozygous 723936555 5 92272505 92272506 C T 13 GENIC homozygous 588991310 5 92272790 92272791 G T 19 GENIC homozygous 588991311 5 92272838 92272839 G T 4 GENIC homozygous 588991312 5 92272913 92272914 A G 11 GENIC homozygous 588991313 5 92273832 92273833 T C 20 GENIC possibly homozygous 590848159 5 92274188 92274189 C T 6 GENIC heterozygous 590848160 5 92274598 92274599 G A 7 GENIC possibly homozygous 590848161 5 92274645 92274646 A C 5 GENIC homozygous 590848162 5 92274922 92274923 A G 12 GENIC homozygous 590848163 5 92275069 92275070 G A 11 GENIC possibly homozygous 590848164 5 92275227 92275228 C T 3 GENIC homozygous 590848165 5 92275714 92275715 T G 14 GENIC homozygous 588991314 5 92276027 92276028 G A 17 GENIC possibly homozygous 588991315 5 92276604 92276605 C G 7 GENIC heterozygous 588991316