chr start stop reference nuc variant nuc depth genic status zygosity variant ID 10 63776106 63776107 G C 8 GENIC homozygous 997918751 10 63776223 63776224 A G 14 GENIC homozygous 997918752 10 63778203 63778204 C A 21 GENIC homozygous 997918753 10 63779688 63779689 C T 7 GENIC homozygous 997918754 10 63779692 63779693 T G 3 GENIC homozygous 997918755 10 63780196 63780197 T G 29 GENIC homozygous 997918756 10 63780252 63780253 G T 33 GENIC homozygous 997918757 10 63780253 63780254 T G 32 GENIC homozygous 997918758 10 63782074 63782075 T C 29 GENIC homozygous 997918759 10 63782946 63782947 C T 19 GENIC possibly homozygous 997918760 10 63784037 63784038 C G 30 GENIC homozygous 997918761 10 63784734 63784735 A T 27 GENIC homozygous 997918762 10 63784855 63784856 G A 37 GENIC homozygous 997918763 10 63789289 63789290 T C 22 GENIC homozygous 997918764 10 63789439 63789440 G T 32 GENIC homozygous 997918765 10 63790620 63790621 A C 6 GENIC homozygous 997918766 10 63790671 63790672 T C 16 GENIC homozygous 997918767 10 63792790 63792791 C T 27 GENIC homozygous 997918768 10 63794661 63794662 G T 18 GENIC homozygous 997918769 10 63794741 63794742 G C 27 GENIC homozygous 997918770 10 63794830 63794831 T G 25 GENIC homozygous 997918771 10 63795014 63795015 T C 27 GENIC homozygous 997918772