chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
17	22137734	22137735	T	TA	36	GENIC	heterozygous	47306296
17	22138048	22138049	C	CT	39	GENIC	homozygous	47052525
17	22138187	22138188	G	A	45	GENIC	homozygous	47052526
17	22138451	22138452	A	G	52	GENIC	homozygous	47052527
17	22138575	22138576	G	A	37	GENIC	homozygous	47306298
17	22138786	22138787	C	T	55	GENIC	homozygous	47306300
17	22141286	22141287	G	A	50	GENIC	homozygous	47306302
17	22141984	22141985	T	TG	1	GENIC	homozygous	47052537
17	22141992	22141993	T	TG	1	GENIC	homozygous	47052538
17	22141999	22142000	T	TG	1	GENIC	homozygous	47052539
17	22142100	22142101	G	T	21	GENIC	homozygous	47306304
17	22142138	22142139	T	C	30	GENIC	possibly homozygous	47052541
17	22142263	22142264	A	T	60	GENIC	homozygous	47306306
17	22142413	22142415	CA	--	1	GENIC	homozygous	47052543
17	22143146	22143147	A	-	29	GENIC	homozygous	47052548
17	22143154	22143155	A	-	25	GENIC	homozygous	47052549
17	22143158	22143159	A	-	24	GENIC	homozygous	47052550
17	22143164	22143165	C	-	26	GENIC	homozygous	47052551
17	22143286	22143287	T	TC	37	GENIC	homozygous	47052552