chr start stop reference nuc variant nuc depth genic status zygosity variant ID 5 92269075 92269076 G T 12 GENIC homozygous 537404660 5 92269612 92269613 C CG 19 GENIC homozygous 697260572 5 92269749 92269750 A G 13 GENIC homozygous 537404661 5 92269820 92269821 C T 12 GENIC homozygous 537404662 5 92270563 92270564 G T 2 GENIC homozygous 537404663 5 92270583 92270588 TTCTG ----- 1 GENIC homozygous 697260573 5 92270723 92270724 T C 13 GENIC homozygous 537404664 5 92271050 92271051 A G 14 GENIC homozygous 537404665 5 92271089 92271090 G A 4 GENIC homozygous 537404666 5 92271322 92271323 T TA 1 GENIC homozygous 697260574 5 92272505 92272506 C T 15 GENIC homozygous 537404667 5 92272790 92272791 G T 22 GENIC possibly homozygous 537404668 5 92272838 92272839 G T 23 GENIC homozygous 537404669 5 92272913 92272914 A G 22 GENIC homozygous 537404670 5 92273832 92273833 T C 11 GENIC possibly homozygous 539687702 5 92274188 92274189 C T 22 GENIC homozygous 539687703 5 92274598 92274599 G A 9 GENIC possibly homozygous 539687704 5 92274645 92274646 A C 9 GENIC homozygous 539687705 5 92274922 92274923 A G 19 GENIC homozygous 539687706 5 92275069 92275070 G A 9 GENIC homozygous 539687707 5 92275227 92275228 C T 15 GENIC possibly homozygous 539687708 5 92275714 92275715 T G 10 GENIC homozygous 537404671 5 92276027 92276028 G A 9 GENIC homozygous 537404672 5 92276604 92276605 C G 30 GENIC homozygous 537404673