chr start stop reference nuc variant nuc depth genic status zygosity variant ID 12 23941489 23941490 G A 32 GENIC homozygous 115286191 12 23942728 23942729 C G 19 GENIC homozygous 115286193 12 23942947 23942948 C T 33 GENIC homozygous 115286195 12 23943269 23943270 G A 31 GENIC homozygous 115469773 12 23943683 23943684 T G 31 GENIC homozygous 115286197 12 23944550 23944551 T A 15 GENIC possibly homozygous 115422062 12 23944835 23944836 T G 33 GENIC homozygous 115286199 12 23945077 23945078 T C 27 GENIC homozygous 115286201 12 23945614 23945615 T C 30 GENIC homozygous 115286205 12 23945914 23945915 C T 21 GENIC homozygous 115286207 12 23946266 23946267 A G 33 GENIC homozygous 115286209 12 23946560 23946561 C T 27 GENIC homozygous 115286213 12 23946574 23946575 T A 26 GENIC homozygous 115438578 12 23946601 23946602 C A 29 GENIC homozygous 115438579 12 23946605 23946606 T C 30 GENIC homozygous 115438580 12 23947790 23947791 A C 30 GENIC homozygous 115286215 12 23947916 23947917 C A 27 GENIC homozygous 115286217 12 23948186 23948187 T A 20 GENIC homozygous 115286219 12 23948728 23948729 C A 30 GENIC possibly homozygous 115286221 12 23948832 23948833 T C 20 GENIC homozygous 115286223 12 23949064 23949065 A C 24 GENIC homozygous 115286225 12 23949295 23949296 T A 27 GENIC homozygous 115286227 12 23949833 23949834 A T 34 GENIC possibly homozygous 115286229 12 23950222 23950223 T C 24 GENIC homozygous 115286231 12 23950339 23950340 C T 27 GENIC homozygous 115286233 12 23951204 23951205 A G 21 GENIC homozygous 115286235 12 23951318 23951319 G A 19 GENIC homozygous 115286237 12 23951823 23951824 C T 40 GENIC homozygous 115286239 12 23952517 23952518 G A 27 GENIC homozygous 115286243