chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
19	25029182	25029183	G	C	22	GENIC	homozygous	109672124
19	25029287	25029288	A	G	35	GENIC	homozygous	109672126
19	25032831	25032832	A	C	12	GENIC	possibly homozygous	109866734
19	25033579	25033580	C	T	35	GENIC	homozygous	109866736
19	25036921	25036922	A	G	24	GENIC	homozygous	109672132
19	25042571	25042572	A	G	22	GENIC	homozygous	109672140
19	25044553	25044554	T	C	20	GENIC	homozygous	109672144
19	25046726	25046727	C	T	26	GENIC	homozygous	109866738
19	25047871	25047872	C	T	36	GENIC	homozygous	109866740
19	25049255	25049256	T	C	32	GENIC	homozygous	109866742
19	25054379	25054380	C	T	26	GENIC	homozygous	109672154
19	25062076	25062077	A	G	29	GENIC	homozygous	109672156
19	25065173	25065174	T	C	34	GENIC	homozygous	109672160
19	25065503	25065504	T	C	26	GENIC	homozygous	109672164
19	25066615	25066616	G	A	24	GENIC	possibly homozygous	109866744
19	25067322	25067323	G	C	24	GENIC	homozygous	109866746