chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
17	9972909	9972910	C	T	37	GENIC	homozygous	110953492
17	9974923	9974924	A	G	30	GENIC	possibly homozygous	110953494
17	9975021	9975022	A	C	40	GENIC	homozygous	110953496
17	9976327	9976328	G	A	52	GENIC	possibly homozygous	111332232
17	9976365	9976366	T	C	52	GENIC	possibly homozygous	111332235
17	9976834	9976835	A	G	54	GENIC	homozygous	110953498
17	9976909	9976910	C	T	62	GENIC	homozygous	110953500
17	9976915	9976916	T	C	62	GENIC	homozygous	110953502
17	9977233	9977234	A	G	54	GENIC	homozygous	111167228
17	9977462	9977463	A	G	35	GENIC	homozygous	110953504
17	9977576	9977577	A	G	46	GENIC	homozygous	110953506
17	9977940	9977941	C	T	56	GENIC	homozygous	110953508
17	9978364	9978365	T	C	56	GENIC	homozygous	111495637
17	9978419	9978420	C	T	27	GENIC	possibly homozygous	119263892
17	9978430	9978431	C	T	22	GENIC	possibly homozygous	119263893
17	9978459	9978460	C	T	45	GENIC	possibly homozygous	119263894
17	9978582	9978583	A	G	65	GENIC	homozygous	110953510
17	9978890	9978891	G	T	60	GENIC	homozygous	110953512
17	9979743	9979744	C	T	35	GENIC	homozygous	110953514
17	9979819	9979820	C	T	44	GENIC	homozygous	110953516
17	9980958	9980959	T	C	21	GENIC	homozygous	111315058
17	9981151	9981152	A	C	27	GENIC	homozygous	110953520
17	9981644	9981645	A	T	55	GENIC	homozygous	110953522
17	9981918	9981919	T	C	45	GENIC	homozygous	110953524
17	9981946	9981947	C	T	26	GENIC	homozygous	110953526
17	9982357	9982358	T	C	50	GENIC	possibly homozygous	119263895
17	9982359	9982360	A	G	52	GENIC	possibly homozygous	119263896
17	9982382	9982383	A	G	54	GENIC	possibly homozygous	119263897
17	9982579	9982580	T	C	65	GENIC	homozygous	110953530