chr start stop reference nuc variant nuc depth genic status zygosity variant ID 1 234676088 234676089 C T 13 GENIC homozygous 109010812 1 234676128 234676129 C A 19 GENIC homozygous 120515783 1 234676143 234676144 C A 23 GENIC homozygous 109010813 1 234679895 234679896 T C 24 GENIC homozygous 109010814 1 234682913 234682913 A 53 GENIC homozygous 130834404 1 234683777 234683778 G T 25 GENIC homozygous 109010816 1 234684266 234684267 C T 28 GENIC homozygous 109010817 1 234690348 234690349 G A 30 GENIC homozygous 109010818 1 234689793 234689794 A G 26 GENIC homozygous 108567265 1 234682913 234682914 T G 55 GENIC homozygous 120492312 1 234689203 234689204 A G 19 GENIC possibly homozygous 120492313 1 234689204 234689205 T A 19 GENIC possibly homozygous 120492314 1 234686648 234686649 G A 21 GENIC homozygous 109202229 1 234686694 234686709 TGCCACACTCGTCAT 14 GENIC homozygous 131264600 1 234694555 234694556 T G 30 GENIC homozygous 109010819 1 234696971 234696972 C A 26 GENIC homozygous 109010820 1 234699695 234699698 TGG 20 GENIC homozygous 131264601 1 234701288 234701289 C A 24 GENIC homozygous 109010821 1 234701464 234701465 T C 21 GENIC homozygous 109010822 1 234702598 234702599 G C 16 GENIC homozygous 109010824 1 234702875 234702876 C T 15 GENIC homozygous 109010825 1 234703570 234703571 G A 19 GENIC homozygous 109010826 1 234703603 234703604 A G 21 GENIC homozygous 109010827 1 234704302 234704303 T C 17 GENIC homozygous 109202231 1 234704652 234704653 A G 16 GENIC homozygous 108567275