chr start stop reference nuc variant nuc depth genic status zygosity variant ID 1 105207501 105207502 A T 26 GENIC possibly homozygous 61491699 1 105207713 105207714 G GTGTGTGTGTGTGTGTGTGTGTGTGTGTGTAT 3 GENIC homozygous 62085483 1 105207883 105207884 T C 18 GENIC homozygous 61737353 1 105212116 105212117 C T 27 GENIC homozygous 61737355 1 105212957 105212958 A G 19 GENIC possibly homozygous 61491720 1 105213674 105213675 C T 27 GENIC homozygous 61737357 1 105213758 105213759 G A 8 GENIC homozygous 61737359 1 105213915 105213916 T G 6 GENIC heterozygous 61737361 1 105214154 105214155 A - 4 GENIC homozygous 61737363 1 105214252 105214253 A G 20 GENIC homozygous 61737365 1 105214335 105214336 G A 6 GENIC homozygous 61737367 1 105214416 105214417 C T 14 GENIC homozygous 61737369 1 105214436 105214437 T G 20 GENIC possibly homozygous 61737371 1 105215229 105215230 G A 8 GENIC homozygous 61737373 1 105219382 105219383 A G 15 GENIC homozygous 61737375 1 105221107 105221108 T TGACA 5 GENIC homozygous 61491736 1 105222120 105222121 C CCTG 3 GENIC homozygous 62085484 1 105222652 105222653 T C 9 GENIC homozygous 61491739 1 105222773 105222774 G C 19 GENIC possibly homozygous 61737377 1 105224362 105224363 T C 23 GENIC possibly homozygous 61737379