chr start stop reference nuc variant nuc depth genic status zygosity variant ID X 15695462 15695463 G GAA 6 GENIC homozygous 45097276 X 15695479 15695480 A - 4 GENIC heterozygous 45097277 X 15695659 15695660 C T 19 GENIC homozygous 45097278 X 15697473 15697474 G A 20 GENIC homozygous 45097279 X 15697497 15697498 G A 20 GENIC homozygous 45097280 X 15699571 15699572 C T 13 GENIC homozygous 45097281 X 15699582 15699583 C G 14 GENIC homozygous 45097282 X 15700996 15700997 T C 9 GENIC homozygous 45097283 X 15701633 15701634 C T 22 GENIC homozygous 45097284 X 15701653 15701654 C T 25 GENIC homozygous 45097285 X 15701906 15701907 T C 7 GENIC homozygous 45097286 X 15702095 15702096 T - 9 GENIC heterozygous 45097287 X 15703931 15703932 T C 13 GENIC homozygous 45097288 X 15706007 15706008 G A 28 GENIC heterozygous 45097289 X 15708086 15708087 C T 3 GENIC homozygous 45097291 X 15708864 15708865 G A 9 GENIC homozygous 45097292 X 15702094 15702096 TT -- 9 GENIC heterozygous 45252066