chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
19	39077754	39077755	C	G	14	GENIC	homozygous	109976925
19	39078039	39078040	G	T	23	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	28	GENIC	homozygous	109816104
19	39081773	39081774	G	T	21	GENIC	homozygous	109869931
19	39081959	39081960	T	C	24	GENIC	homozygous	109816106
19	39083002	39083003	C	G	30	GENIC	homozygous	109816110
19	39083360	39083361	T	C	22	GENIC	homozygous	109816112
19	39086034	39086035	T	G	15	GENIC	homozygous	109925884
19	39086087	39086088	A	G	15	GENIC	homozygous	110065578
19	39087082	39087083	C	T	30	GENIC	homozygous	109816114
19	39087115	39087116	C	T	26	GENIC	homozygous	109816116