chr start stop reference nuc variant nuc depth genic status zygosity variant ID 1 263812471 263812472 G A 71 GENIC homozygous 773964245 1 263813164 263813165 C A 44 GENIC homozygous 773964246 1 263813492 263813493 T A 39 GENIC homozygous 773964247 1 263814011 263814012 C T 38 GENIC homozygous 773964248 1 263814051 263814052 C T 42 GENIC homozygous 773964249 1 263814338 263814339 G A 48 GENIC homozygous 773964250 1 263815026 263815027 C T 29 GENIC homozygous 773964251 1 263815349 263815350 G A 37 GENIC possibly homozygous 773964252 1 263815744 263815745 A G 43 GENIC homozygous 773964253 1 263817320 263817321 G A 35 GENIC homozygous 773964254 1 263817743 263817744 A G 60 GENIC homozygous 773964255 1 263818715 263818716 G A 23 GENIC homozygous 773964256 1 263819181 263819182 C T 28 GENIC homozygous 773964257 1 263820712 263820713 T C 34 GENIC possibly homozygous 773964258 1 263820813 263820814 A G 30 GENIC homozygous 773964259 1 263820861 263820862 C T 28 GENIC homozygous 773964260 1 263823243 263823244 C T 59 GENIC homozygous 773964261 1 263825226 263825227 C T 41 GENIC heterozygous 773964262 1 263825765 263825766 G T 29 GENIC possibly homozygous 773964263 1 263826119 263826120 G A 47 GENIC homozygous 773964264 1 263827331 263827332 G A 37 GENIC homozygous 773964265 1 263828502 263828503 C A 42 GENIC homozygous 773964266 1 263830697 263830698 G A 27 GENIC homozygous 773964267 1 263831722 263831723 C T 19 GENIC possibly homozygous 773964268 1 263832813 263832814 A G 23 GENIC homozygous 773964269 1 263835278 263835279 C T 29 GENIC homozygous 773964270 1 263835926 263835927 G A 16 GENIC homozygous 773964271 1 263840399 263840400 G A 46 GENIC homozygous 773964272 1 263843300 263843301 A T 19 GENIC homozygous 773964273