chr start stop reference nuc variant nuc depth genic status zygosity variant ID X 10023747 10023748 C T 13 GENIC homozygous 108223832 X 10024674 10024675 C T 11 GENIC homozygous 108223834 X 10025405 10025406 G A 9 GENIC homozygous 108223836 X 10028572 10028573 A G 19 GENIC homozygous 108223838 X 10031058 10031059 T C 12 GENIC homozygous 108223840 X 10031435 10031436 G A 12 GENIC homozygous 108223842 X 10031910 10031911 T C 9 GENIC homozygous 108223844 X 10032106 10032107 A G 4 GENIC homozygous 108223846 X 10032410 10032411 G A 7 GENIC homozygous 108223848 X 10032505 10032506 A G 3 GENIC homozygous 108223850 X 10034063 10034064 G C 3 GENIC homozygous 108223853 X 10035255 10035256 G A 4 GENIC homozygous 108223855 X 10035464 10035465 A C 11 GENIC homozygous 108223857 X 10037290 10037291 T C 4 GENIC homozygous 108223859 X 10037549 10037550 A G 12 GENIC homozygous 108223861 X 10038584 10038585 T C 7 GENIC homozygous 108223863 X 10039566 10039567 T C 18 GENIC homozygous 108223865 X 10039606 10039607 A G 11 GENIC homozygous 108223867 X 10040929 10040930 C T 11 GENIC homozygous 108223869 X 10041859 10041860 G C 10 GENIC homozygous 108223871 X 10043326 10043327 A G 8 GENIC homozygous 108223873