chr start stop reference nuc variant nuc depth genic status zygosity variant ID X 46978965 46978966 G T 39 GENIC homozygous 783292026 X 46990278 46990279 G T 22 GENIC homozygous 783292027 X 46990372 46990373 G T 62 GENIC possibly homozygous 783292028 X 46990416 46990417 T G 64 GENIC homozygous 783292029 X 46999527 46999528 T A 53 GENIC heterozygous 783292030 X 46999533 46999534 A T 54 GENIC heterozygous 783292031 X 47003499 47003500 T A 13 GENIC homozygous 783292032 X 47003541 47003542 T A 28 GENIC homozygous 783292033 X 47003581 47003582 C T 25 GENIC homozygous 783292034 X 47003610 47003611 G T 14 GENIC homozygous 783292035 X 47003652 47003653 C A 22 GENIC homozygous 783292036 X 47003804 47003805 C A 13 GENIC homozygous 783292037 X 47016754 47016755 T A 68 GENIC homozygous 783292038