chr start stop reference nuc variant nuc depth genic status zygosity variant ID 5 92269075 92269076 G T 27 GENIC possibly homozygous 656173337 5 92269612 92269613 C CG 25 GENIC homozygous 760719342 5 92269820 92269821 C T 26 GENIC homozygous 656173338 5 92270228 92270229 G A 14 GENIC homozygous 656173339 5 92270563 92270564 G T 21 GENIC possibly homozygous 656173340 5 92270583 92270588 TTCTG ----- 21 GENIC possibly homozygous 760719343 5 92270723 92270724 T C 15 GENIC homozygous 656173341 5 92271050 92271051 A G 25 GENIC homozygous 656173342 5 92271089 92271090 G A 25 GENIC homozygous 656173343 5 92271322 92271323 T TA 13 GENIC homozygous 760719344 5 92272505 92272506 C T 29 GENIC homozygous 656173344 5 92272790 92272791 G T 21 GENIC possibly homozygous 656173345 5 92272838 92272839 G T 20 GENIC homozygous 656173346 5 92272913 92272914 A G 33 GENIC homozygous 656173347 5 92273832 92273833 T C 17 GENIC homozygous 656173348 5 92274188 92274189 C T 22 GENIC homozygous 656173349 5 92274598 92274599 G A 31 GENIC homozygous 656173350 5 92274645 92274646 A C 24 GENIC homozygous 656173351 5 92274922 92274923 A G 24 GENIC homozygous 656173352 5 92275069 92275070 G A 26 GENIC homozygous 656173353 5 92275714 92275715 T G 26 GENIC homozygous 656173354 5 92276027 92276028 G A 11 GENIC homozygous 656173355 5 92276604 92276605 C G 21 GENIC homozygous 656173356