chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
19	11389728	11389728		ACGTACCAG	49	GENIC	homozygous	129584417
19	11389733	11389733		T	52	GENIC	homozygous	129584418
19	11389835	11389836	C	G	55	GENIC	homozygous	109636570
19	11389842	11389842		G	52	GENIC	homozygous	129584419
19	11389910	11389911	A		40	GENIC	homozygous	129584420
19	11389929	11389929		T	44	GENIC	homozygous	129584421
19	11389935	11389936	T	G	45	GENIC	homozygous	109636572
19	11389954	11389955	T	G	43	GENIC	homozygous	109636574
19	11389958	11389959	C		46	GENIC	homozygous	129584422
19	11389990	11389992	TC		44	GENIC	homozygous	129584423
19	11390029	11390029		C	45	GENIC	homozygous	129584424
19	11390062	11390063	A		41	GENIC	homozygous	129584425
19	11390099	11390099		T	45	GENIC	homozygous	129584426
19	11390107	11390107		T	46	GENIC	homozygous	129584427
19	11390148	11390148		G	38	GENIC	homozygous	129584428
19	11390165	11390166	A		36	GENIC	homozygous	129584429
19	11390192	11390192		G	33	GENIC	homozygous	129584430
19	11394289	11394290	T	C	15	GENIC	homozygous	119596655
19	11393481	11393482	C	T	53	GENIC	homozygous	109764841
19	11398353	11398354	C	T	19	GENIC	homozygous	109887088
19	11398361	11398362	A	T	17	GENIC	homozygous	109887090
19	11398368	11398369	C	T	16	GENIC	homozygous	109887092
19	11398381	11398382	A	T	13	GENIC	homozygous	109887094
19	11398394	11398395	G	T	10	GENIC	homozygous	109799592
19	11411646	11411647	A	G	51	GENIC	homozygous	109636578
19	11412697	11412698	C	T	58	GENIC	possibly homozygous	109636581
19	11415376	11415377	C	G	47	GENIC	homozygous	109636583
19	11415392	11415393	C	A	45	GENIC	homozygous	109636585
19	11415576	11415577	A	G	44	GENIC	homozygous	109636587