chr start stop reference nuc variant nuc depth genic status zygosity variant ID 2 143096275 143096276 T C 29 GENIC homozygous 120446124 2 143098400 143098401 T G 35 GENIC possibly homozygous 120206569 2 143097303 143097304 T C 22 GENIC homozygous 110973713 2 143097773 143097774 T C 24 GENIC possibly homozygous 110973715 2 143098877 143098878 A G 18 GENIC possibly homozygous 120206571 2 143099065 143099066 A G 12 GENIC homozygous 110973721 2 143099389 143099390 G A 23 GENIC possibly homozygous 110973723 2 143099829 143099830 C T 12 GENIC homozygous 120206581 2 143100215 143100216 C T 21 GENIC possibly homozygous 120446125 2 143100258 143100259 C T 20 GENIC homozygous 120446126 2 143102714 143102715 G C 29 GENIC possibly homozygous 110973727 2 143102782 143102783 C T 29 GENIC homozygous 110973729 2 143102941 143102942 C T 21 GENIC homozygous 110973731 2 143102944 143102945 C T 23 GENIC homozygous 110973733 2 143103671 143103672 A G 25 GENIC homozygous 120206626