chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
19	25930015	25930016	G	T	34	GENIC	possibly homozygous	109888304
19	25930090	25930091	G	C	25	GENIC	homozygous	109867616
19	25931409	25931410	C	T	29	GENIC	homozygous	109867618
19	25931444	25931445	A	G	33	GENIC	homozygous	109867620
19	25931591	25931592	C	T	16	GENIC	homozygous	109867622
19	25932526	25932527	A	G	21	GENIC	homozygous	109673515
19	25932695	25932696	C	T	20	GENIC	homozygous	109867624
19	25933177	25933178	T	C	33	GENIC	homozygous	109867626
19	25933384	25933385	G	A	23	GENIC	homozygous	109867628
19	25934591	25934592	T	C	19	GENIC	homozygous	109867630
19	25935951	25935952	T	C	14	GENIC	homozygous	109867632
19	25936160	25936161	A	G	14	GENIC	homozygous	109867634
19	25936809	25936810	T	C	23	GENIC	homozygous	109673517