chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
3	41690077	41690077		TA	19	GENIC	homozygous	143854873
3	41691948	41691949	C	T	18	GENIC	homozygous	143881113
3	41692866	41692867	T	C	22	GENIC	homozygous	143881114
3	41693830	41693830		TG	16	GENIC	homozygous	143854874
3	41695834	41695835	T	C	11	GENIC	homozygous	143881115
3	41696847	41696848	C	T	22	GENIC	homozygous	143881116
3	41697026	41697027	T	A	12	GENIC	homozygous	143881117
3	41698475	41698476	T	C	16	GENIC	homozygous	143881118
3	41699217	41699309	GTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGCAATGTACAGTTCGGCCCCCTCTCGGTGATCCTAGCTGCCCGGGCGAGCGGTTGG		4	GENIC	homozygous	143854875
3	41699621	41699622	T	A	17	GENIC	homozygous	143881119
3	41702055	41702056	T		18	GENIC	possibly homozygous	143854876
3	41704138	41704139	G	T	22	GENIC	homozygous	143881120
3	41704247	41704247		T	19	GENIC	homozygous	143854877
3	41704606	41704607	C	T	19	GENIC	homozygous	143881121
3	41706704	41706705	G	T	19	GENIC	homozygous	143881122
3	41706814	41706815	A	G	15	GENIC	homozygous	143881123
3	41695834	41695835	T		11	GENIC	heterozygous	403885557
3	41699205	41699206	G	A	7	GENIC	heterozygous	154094096
3	41699205	41699206	G		7	GENIC	heterozygous	403924515