chr start stop reference nuc variant nuc depth genic status zygosity variant ID 17 10539576 10539577 A G 30 GENIC homozygous 974057826 17 10542421 10542422 A G 27 GENIC homozygous 974057827 17 10542745 10542746 T C 41 GENIC homozygous 974057828 17 10543058 10543059 T C 32 GENIC homozygous 974057829 17 10543406 10543407 C T 22 GENIC possibly homozygous 974057830 17 10543603 10543604 A G 19 GENIC homozygous 974057831 17 10543768 10543769 C G 12 GENIC homozygous 974057832 17 10544550 10544551 T C 19 GENIC homozygous 974057833 17 10545067 10545068 A G 25 GENIC homozygous 974057834 17 10545861 10545862 C T 14 GENIC homozygous 974057835 17 10546825 10546826 A G 26 GENIC homozygous 974057836 17 10546960 10546961 T C 26 GENIC possibly homozygous 974057837 17 10547488 10547489 G A 39 GENIC homozygous 974057838