chr start stop reference nuc variant nuc depth genic status zygosity variant ID 10 92025498 92025499 C T 28 GENIC homozygous 991596582 10 92026302 92026303 C T 18 GENIC homozygous 991596583 10 92026777 92026778 C T 20 GENIC homozygous 991596584 10 92028059 92028060 T A 33 GENIC homozygous 991596585 10 92028106 92028107 A G 17 GENIC homozygous 991596586 10 92029769 92029770 A G 8 GENIC homozygous 991596587 10 92029782 92029783 G A 5 GENIC homozygous 991596588 10 92029897 92029898 A G 13 GENIC homozygous 991596589 10 92029899 92029900 G T 14 GENIC homozygous 991596590 10 92030733 92030734 T C 18 GENIC homozygous 991596591 10 92031467 92031468 G C 23 GENIC homozygous 991596592 10 92031653 92031654 T C 19 GENIC homozygous 991596593 10 92032722 92032723 C A 18 GENIC homozygous 991596594 10 92032794 92032795 C T 14 GENIC homozygous 991596595 10 92033006 92033007 T C 17 GENIC homozygous 991596596 10 92034140 92034141 C G 19 GENIC homozygous 991596597 10 92034438 92034439 C T 28 GENIC homozygous 991596598 10 92035331 92035332 C G 14 GENIC homozygous 991596599 10 92037326 92037327 C T 27 GENIC homozygous 991596600 10 92037519 92037520 T C 8 GENIC homozygous 991596601 10 92039540 92039541 G T 18 GENIC homozygous 991596602 10 92040134 92040135 C T 21 GENIC homozygous 991596603