chr start stop reference nuc variant nuc depth genic status zygosity variant ID 17 14311702 14311703 C T 20 GENIC homozygous 119329487 17 14312139 14312140 G C 60 GENIC homozygous 111335998 17 14312218 14312219 T G 50 GENIC homozygous 119329488 17 14312220 14312221 A C 48 GENIC possibly homozygous 119329489 17 14312221 14312222 T C 48 GENIC homozygous 119329490 17 14312288 14312289 C T 61 GENIC homozygous 119329491 17 14312301 14312302 T C 55 GENIC possibly homozygous 119329492 17 14312483 14312484 C T 38 GENIC homozygous 119329493 17 14317933 14317934 G A 54 GENIC heterozygous 119329494 17 14319658 14319659 G T 124 GENIC heterozygous 119329495 17 14319734 14319735 G A 126 GENIC heterozygous 119329496 17 14319797 14319798 T C 112 GENIC possibly homozygous 111336002 17 14319803 14319804 G C 108 GENIC heterozygous 119329497 17 14319855 14319856 T C 86 GENIC heterozygous 111336004 17 14319732 14319733 G A 125 GENIC heterozygous 119265913 17 14319948 14319949 G T 69 GENIC heterozygous 119265914 17 14319985 14319986 A G 54 GENIC heterozygous 119265916