chr start stop reference nuc variant nuc depth genic status zygosity variant ID 9 9579472 9579473 C T 42 GENIC homozygous 539556760 9 9582667 9582668 G - 2 GENIC homozygous 697582818 9 9585458 9585459 T TC 16 GENIC possibly homozygous 697582819 9 9587121 9587122 C T 3 GENIC homozygous 539556761 9 9587145 9587146 C T 4 GENIC heterozygous 539556762 9 9587150 9587151 C T 4 GENIC heterozygous 539556763 9 9588104 9588105 C T 38 GENIC homozygous 539556764 9 9588458 9588459 A C 35 GENIC homozygous 539556765 9 9589184 9589185 G - 30 GENIC homozygous 697582820 9 9594207 9594208 G GT 15 GENIC homozygous 697582821 9 9600833 9600834 C - 30 GENIC homozygous 697582822 9 9603609 9603610 T C 35 GENIC homozygous 539556766 9 9607624 9607625 G GA 19 GENIC possibly homozygous 697582823 9 9613557 9613558 T TC 30 GENIC homozygous 697582825 9 9614339 9614340 C CTG 3 GENIC homozygous 697582827 9 9614980 9614982 TT -- 16 GENIC homozygous 697582828 9 9615005 9615006 C T 17 GENIC homozygous 539556767 9 9615386 9615387 A T 54 GENIC homozygous 539556768 9 9617303 9617304 A - 23 GENIC homozygous 697582830 9 9619579 9619580 C CCA 23 GENIC homozygous 697582831 9 9619582 9619583 G - 18 GENIC homozygous 697582832 9 9619584 9619585 T TCA 20 GENIC homozygous 697582833 9 9620520 9620521 A G 39 GENIC homozygous 539556769 9 9625193 9625194 T G 16 GENIC homozygous 539556770 9 9625202 9625203 C CT 10 GENIC possibly homozygous 697582834 9 9625238 9625240 TT -- 4 GENIC heterozygous 697582835 9 9626809 9626810 A C 18 GENIC homozygous 539556771 9 9626982 9626989 GCCCCGG ------- 8 GENIC possibly homozygous 697582837 9 9627023 9627024 A AGTCTCG 19 GENIC possibly homozygous 697582838 9 9632720 9632721 A G 36 GENIC homozygous 539556772 9 9634070 9634071 C - 26 GENIC heterozygous 697582839 9 9634084 9634085 C A 23 GENIC possibly homozygous 539556773 9 9637244 9637245 C A 26 GENIC homozygous 539556774