chr start stop reference nuc variant nuc depth genic status zygosity variant ID 12 24136858 24136859 A C 8 GENIC homozygous 941913072 12 24139631 24139632 A T 14 GENIC homozygous 941913073 12 24142950 24142951 C T 28 GENIC homozygous 941913074 12 24144974 24144975 T C 7 GENIC homozygous 941913075 12 24150499 24150500 T C 29 GENIC homozygous 941913076 12 24150704 24150705 T C 29 GENIC homozygous 941913077 12 24150783 24150784 G T 29 GENIC homozygous 941913078 12 24150797 24150798 G A 34 GENIC homozygous 941913079 12 24150901 24150902 G T 30 GENIC homozygous 941913080 12 24150985 24150986 G A 17 GENIC homozygous 941913081 12 24151074 24151075 T C 30 GENIC homozygous 941913082 12 24151224 24151225 C A 29 GENIC homozygous 941913083 12 24151231 24151232 C A 29 GENIC homozygous 941913084 12 24151239 24151240 G C 26 GENIC homozygous 941913085 12 24151281 24151282 T C 22 GENIC homozygous 941913086 12 24151455 24151456 A G 36 GENIC homozygous 941913087 12 24151547 24151548 A G 30 GENIC homozygous 941913088 12 24151550 24151551 T G 29 GENIC homozygous 941913089 12 24151560 24151561 T C 32 GENIC homozygous 941913090 12 24151661 24151662 T G 23 GENIC homozygous 941913091 12 24151782 24151783 A G 26 GENIC homozygous 941913092 12 24151889 24151890 G A 23 GENIC homozygous 941913093 12 24151893 24151894 C T 25 GENIC homozygous 941913094 12 24152060 24152061 G A 21 GENIC homozygous 941913095 12 24152087 24152088 C T 18 GENIC homozygous 941913096 12 24152559 24152560 C T 21 GENIC homozygous 941913097