chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
3	129652598	129652599	T	C	20	GENIC	homozygous	57670469
3	129652599	129652600	G	A	20	GENIC	homozygous	57670471
3	129653298	129653299	G	A	15	GENIC	homozygous	57670473
3	129653987	129653988	C	T	22	GENIC	homozygous	57670475
3	129654838	129654839	G	A	15	GENIC	homozygous	57670479
3	129656308	129656325	CAGGTCCCCCGGAAAGG	-----------------	11	GENIC	homozygous	57670481
3	129656985	129656986	G	A	17	GENIC	homozygous	57670483
3	129657111	129657112	C	T	19	GENIC	homozygous	57670485
3	129658097	129658098	A	AT	16	GENIC	homozygous	57670487
3	129659438	129659439	C	T	13	GENIC	homozygous	57670491
3	129660226	129660227	T	-	18	GENIC	possibly homozygous	57670495
3	129661042	129661043	C	T	8	GENIC	homozygous	57670497
3	129663140	129663141	G	A	21	GENIC	homozygous	57670499
3	129665568	129665569	C	G	11	GENIC	homozygous	57670503
3	129666506	129666507	A	T	11	GENIC	homozygous	57670505
3	129668229	129668230	C	T	15	GENIC	homozygous	57670509
3	129669216	129669217	G	A	18	GENIC	homozygous	57670517
3	129669784	129669785	C	T	12	GENIC	homozygous	57670519
3	129659588	129659589	G	C	13	GENIC	homozygous	58560480