chr start stop reference nuc variant nuc depth genic status zygosity variant ID X 44961339 44961340 T C 19 GENIC homozygous 108489565 X 44962703 44962704 A C 14 GENIC homozygous 108489567 X 44963038 44963039 C T 13 GENIC homozygous 108489569 X 44964109 44964110 T G 14 GENIC homozygous 108489571 X 44967164 44967165 A G 6 GENIC homozygous 108489573 X 44967280 44967281 T C 5 GENIC homozygous 108489575 X 44967807 44967808 T C 19 GENIC homozygous 108489577 X 44969422 44969423 T C 17 GENIC homozygous 108489579 X 44969522 44969523 C A 18 GENIC homozygous 108489581 X 44972807 44972808 C T 19 GENIC homozygous 108489583 X 44974820 44974821 C T 16 GENIC homozygous 108489585 X 44975520 44975521 T G 12 GENIC homozygous 108489587 X 44975556 44975557 A G 10 GENIC homozygous 108489589 X 44979363 44979364 A G 12 GENIC homozygous 108489591 X 44979739 44979740 C T 7 GENIC homozygous 108489593 X 44980761 44980762 C T 8 GENIC homozygous 108489595 X 44981796 44981797 A C 11 GENIC homozygous 108489597 X 44982350 44982351 C A 16 GENIC homozygous 108489599 X 44986394 44986395 C A 6 GENIC homozygous 108489601