chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
19	42101587	42101588	A	G	16	GENIC	homozygous	125266029
19	42102154	42102155	C	T	11	GENIC	homozygous	125266030
19	42102686	42102687	G	T	23	GENIC	homozygous	125266031
19	42102787	42102788	A	G	20	GENIC	homozygous	125266032
19	42103725	42103726	G	A	6	GENIC	homozygous	125287461
19	42103873	42103874	G	A	19	GENIC	homozygous	125266033
19	42106313	42106314	G	T	18	GENIC	homozygous	125266034
19	42107599	42107600	C	T	18	GENIC	homozygous	125266035
19	42108806	42108807	T	C	15	GENIC	homozygous	125266036
19	42109092	42109093	G	A	25	GENIC	homozygous	125266037
19	42109437	42109438	A	G	17	GENIC	homozygous	125266038
19	42109880	42109881	C	T	27	GENIC	homozygous	125266039
19	42110121	42110122	G	C	9	GENIC	homozygous	125266040
19	42104891	42104892	C	A	24	GENIC	homozygous	125247953
19	42109051	42109052	C	T	19	GENIC	homozygous	125247954