chr start stop reference nuc variant nuc depth genic status zygosity variant ID 12 19574352 19574353 T C 23 GENIC homozygous 115279380 12 19575393 19575394 T A 28 GENIC homozygous 115279382 12 19575632 19575633 C T 22 GENIC homozygous 115279384 12 19575673 19575674 A C 22 GENIC homozygous 115279386 12 19575953 19575954 A G 29 GENIC homozygous 115279388 12 19576172 19576173 G A 28 GENIC homozygous 115279390 12 19576437 19576438 C T 24 GENIC possibly homozygous 115279392 12 19576440 19576441 G T 23 GENIC possibly homozygous 118248745 12 19576483 19576484 G A 20 GENIC homozygous 118248746 12 19576488 19576489 G A 20 GENIC homozygous 118248748 12 19576506 19576507 C G 15 GENIC homozygous 118248750 12 19576768 19576769 G A 28 GENIC homozygous 115279394 12 19576819 19576820 C T 25 GENIC homozygous 115279396 12 19576864 19576865 C T 24 GENIC homozygous 115279397 12 19576873 19576874 C T 25 GENIC homozygous 115279399 12 19576932 19576933 A G 21 GENIC homozygous 115279401 12 19577491 19577492 T C 20 GENIC homozygous 115279403 12 19576442 19576443 C T 23 GENIC possibly homozygous 115581168 12 19576780 19576780 GTGTAAAG 27 GENIC homozygous 128968818