chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
19	30375075	30375076	A	ATT	4	GENIC	homozygous	46209325
19	30375897	30375898	C	G	11	GENIC	homozygous	46090475
19	30375902	30375903	T	G	6	GENIC	heterozygous	46090476
19	30375905	30375906	T	G	6	GENIC	homozygous	46090477
19	30375940	30375941	T	G	3	GENIC	homozygous	46090478
19	30376018	30376019	T	G	2	GENIC	homozygous	46209326
19	30376114	30376115	A	C	23	GENIC	homozygous	46209327
19	30376115	30376116	A	C	23	GENIC	homozygous	46209328
19	30376950	30376951	C	G	27	GENIC	possibly homozygous	46090479
19	30378218	30378219	T	C	8	GENIC	homozygous	46090480
19	30378222	30378223	T	C	8	GENIC	homozygous	46090481
19	30378242	30378243	T	C	15	GENIC	possibly homozygous	46090482
19	30380756	30380757	A	C	65	GENIC	homozygous	46090483
19	30388976	30388977	C	CT	22	GENIC	heterozygous	46209329
19	30388993	30388994	C	T	45	GENIC	heterozygous	46209330