chr start stop reference nuc variant nuc depth genic status zygosity variant ID X 10197604 10197605 C T 25 GENIC homozygous 108224077 X 10197807 10197808 T C 28 GENIC homozygous 108224079 X 10198567 10198568 A G 29 GENIC homozygous 108224081 X 10202919 10202920 C T 25 GENIC homozygous 108224083 X 10203452 10203453 T C 27 GENIC homozygous 108224085 X 10204481 10204482 G A 28 GENIC homozygous 108224087 X 10204650 10204651 G A 20 GENIC homozygous 108224089 X 10206555 10206556 G T 22 GENIC homozygous 108224091 X 10209075 10209076 A G 21 GENIC homozygous 108224093 X 10209267 10209268 G A 20 GENIC homozygous 108224095 X 10209681 10209682 G A 25 GENIC homozygous 108224097 X 10209811 10209812 G A 26 GENIC homozygous 108224099 X 10210001 10210002 C T 32 GENIC homozygous 108224101 X 10210828 10210829 G A 27 GENIC homozygous 108224103 X 10210844 10210845 C G 30 GENIC homozygous 108224105 X 10211934 10211935 A T 20 GENIC homozygous 108224107 X 10212014 10212015 T A 26 GENIC homozygous 108224109 X 10212151 10212152 C T 17 GENIC homozygous 108224112 X 10213116 10213117 T C 35 GENIC homozygous 108224114 X 10215609 10215610 C T 18 GENIC homozygous 108224116 X 10217771 10217772 A G 24 GENIC homozygous 108224118 X 10200178 10200179 T 22 GENIC homozygous 129719527 X 10214963 10214965 GT 8 GENIC homozygous 129719528 X 10217809 10217809 A 18 GENIC homozygous 129719530 X 10217176 10217177 A G 28 GENIC homozygous 108366665