chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
19	30803901	30803901		T	27	GENIC	homozygous	129600562
19	30811830	30811831	G		19	GENIC	homozygous	129600568
19	30815985	30815986	C		12	GENIC	homozygous	130480210
19	30816006	30816007	C		10	GENIC	homozygous	130480211
19	30816023	30816024	T	C	7	GENIC	homozygous	130488364
19	30816026	30816026		C	8	GENIC	homozygous	130480212
19	30816029	30816029		C	8	GENIC	homozygous	130480213
19	30816046	30816046		C	7	GENIC	homozygous	130480214
19	30816055	30816057	CT		8	GENIC	homozygous	130480215
19	30816062	30816063	G		8	GENIC	homozygous	130480216
19	30816066	30816066		T	8	GENIC	homozygous	130480217
19	30816069	30816069		C	8	GENIC	homozygous	130480218
19	30816080	30816080		C	7	GENIC	homozygous	130480219
19	30816092	30816092		CC	7	GENIC	homozygous	130480220
19	30820419	30820421	TG		20	GENIC	heterozygous	130713759
19	30816033	30816034	A	C	8	GENIC	homozygous	119643282
19	30872843	30872844	G	T	21	GENIC	possibly homozygous	109678821
19	30880269	30880269		T	23	GENIC	homozygous	129600603
19	30884115	30884116	T		10	GENIC	homozygous	129600607
19	30884134	30884135	G		7	GENIC	homozygous	129600608
19	30884166	30884166		G	3	GENIC	homozygous	129600609
19	30893352	30893353	A		15	GENIC	heterozygous	129600625