chr start stop reference nuc variant nuc depth genic status zygosity variant ID 13 89726258 89726259 G A 5 GENIC homozygous 1001480731 13 89727003 89727004 C T 8 GENIC homozygous 1001480732 13 89727289 89727290 C T 11 GENIC homozygous 1001480733 13 89728199 89728200 A G 8 GENIC homozygous 1001480734 13 89728283 89728284 G A 8 GENIC homozygous 1001480735 13 89728524 89728525 A G 8 GENIC homozygous 1001480736 13 89728997 89728998 A G 4 GENIC homozygous 1001480737 13 89729103 89729104 G A 5 GENIC homozygous 1001480738 13 89730067 89730068 G A 5 GENIC homozygous 1001480739 13 89731038 89731039 T A 2 GENIC homozygous 1001480740 13 89733523 89733524 A G 3 GENIC homozygous 1001480741 13 89735314 89735315 T C 2 GENIC homozygous 1001480742 13 89736067 89736068 G C 11 GENIC homozygous 1001480743 13 89736970 89736971 A T 5 GENIC homozygous 1001480744 13 89738441 89738442 C G 5 GENIC homozygous 1001480745 13 89740874 89740875 T C 4 GENIC homozygous 1001480746 13 89740981 89740982 T G 3 GENIC homozygous 1001480747 13 89741383 89741384 C G 7 GENIC homozygous 1001480748 13 89742437 89742438 C T 8 GENIC homozygous 1001480749 13 89743353 89743354 C T 13 GENIC homozygous 1001480750