chr start stop reference nuc variant nuc depth genic status zygosity variant ID X 105293208 105293209 A G 52 GENIC homozygous 796748905 X 105293226 105293227 G A 49 GENIC homozygous 796748906 X 105293276 105293277 G A 35 GENIC homozygous 796748907 X 105293676 105293677 G C 46 GENIC homozygous 796748908 X 105294042 105294043 A G 14 GENIC homozygous 796748909 X 105296887 105296888 T A 53 GENIC homozygous 796748910 X 105297118 105297119 C T 42 GENIC homozygous 796748911 X 105297905 105297906 T A 44 GENIC homozygous 796748912 X 105298659 105298660 A C 41 GENIC possibly homozygous 796748913 X 105301990 105301991 G T 18 GENIC homozygous 796748914 X 105302163 105302164 C A 44 GENIC homozygous 796748915 X 105302184 105302185 T C 51 GENIC homozygous 796748916 X 105302210 105302211 C A 55 GENIC homozygous 796748917 X 105303915 105303916 A G 24 GENIC homozygous 796748918 X 105304541 105304542 A G 6 GENIC homozygous 796748919