chr start stop reference nuc variant nuc depth genic status zygosity variant ID 10 85032943 85032944 T C 34 GENIC homozygous 116665077 10 85033027 85033028 C A 30 GENIC homozygous 117133691 10 85034892 85034893 C T 19 GENIC homozygous 117018732 10 85034907 85034908 G C 22 GENIC homozygous 117226836 10 85037140 85037141 C T 28 GENIC possibly homozygous 117226838 10 85037635 85037636 A G 19 GENIC homozygous 116814848 10 85037772 85037773 C T 24 GENIC homozygous 117018735 10 85038507 85038508 A G 33 GENIC homozygous 117018736 10 85038593 85038594 C T 39 GENIC homozygous 117226840 10 85038617 85038618 G A 35 GENIC homozygous 117018737 10 85039964 85039965 G A 17 GENIC homozygous 117226842 10 85040271 85040272 T C 23 GENIC homozygous 117226844 10 85041566 85041567 T C 19 GENIC homozygous 116665090 10 85041679 85041680 C T 18 GENIC homozygous 117226846 10 85041965 85041966 T C 28 GENIC homozygous 117226848 10 85042217 85042218 A G 19 GENIC homozygous 117018738 10 85042720 85042721 C T 14 GENIC homozygous 117226850 10 85042796 85042797 A G 10 GENIC homozygous 116665092 10 85043106 85043107 C T 23 GENIC homozygous 117226852 10 85044864 85044865 C T 17 GENIC homozygous 116665094 10 85045794 85045795 A G 21 GENIC homozygous 116665096 10 85046243 85046244 C T 18 GENIC homozygous 117226854 10 85046253 85046254 C T 20 GENIC homozygous 117226856 10 85048846 85048847 G C 33 GENIC homozygous 117226858 10 85049089 85049090 G A 28 GENIC homozygous 116665098