chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
19	39078039	39078040	G	T	22	GENIC	homozygous	109816098
19	39078404	39078405	A	G	18	GENIC	homozygous	109816100
19	39081168	39081169	A	G	29	GENIC	homozygous	109816102
19	39081570	39081571	T	C	27	GENIC	homozygous	109816104
19	39081749	39081750	T	C	19	GENIC	homozygous	109869929
19	39081773	39081774	G	T	18	GENIC	homozygous	109869931
19	39081959	39081960	T	C	24	GENIC	homozygous	109816106
19	39082608	39082609	G	A	22	GENIC	homozygous	109816108
19	39083002	39083003	C	G	30	GENIC	homozygous	109816110
19	39083360	39083361	T	C	22	GENIC	homozygous	109816112
19	39087082	39087083	C	T	29	GENIC	homozygous	109816114
19	39087115	39087116	C	T	24	GENIC	homozygous	109816116