chr start stop reference nuc variant nuc depth genic status zygosity variant ID 13 89726013 89726014 G A 50 GENIC homozygous 782036360 13 89726240 89726241 T C 44 GENIC homozygous 782036361 13 89726258 89726259 G A 41 GENIC homozygous 782036362 13 89726601 89726602 C T 50 GENIC homozygous 782036363 13 89728283 89728284 G A 81 GENIC possibly homozygous 782036364 13 89728524 89728525 A G 44 GENIC homozygous 782036365 13 89729103 89729104 G A 54 GENIC homozygous 782036366 13 89730202 89730203 C T 53 GENIC homozygous 782036367 13 89730996 89730997 G T 30 GENIC homozygous 782036368 13 89731187 89731188 G C 17 GENIC possibly homozygous 782036369 13 89731199 89731200 A T 26 GENIC heterozygous 782036370 13 89731203 89731204 T C 24 GENIC heterozygous 782036371 13 89731214 89731215 G T 31 GENIC possibly homozygous 782036372 13 89738441 89738442 C G 55 GENIC possibly homozygous 782036373 13 89738768 89738769 G T 56 GENIC homozygous 782036374 13 89739724 89739725 G T 30 GENIC homozygous 782036375 13 89740874 89740875 T C 70 GENIC homozygous 782036376 13 89740981 89740982 T G 56 GENIC homozygous 782036377 13 89742658 89742659 A G 48 GENIC possibly homozygous 782036378