chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
19	39063507	39063508	T	A	18	GENIC	homozygous	109816063
19	39067727	39067728	C	T	13	GENIC	homozygous	109816065
19	39072907	39072908	T	A	21	GENIC	homozygous	109816067
19	39073275	39073276	A	C	25	GENIC	homozygous	109816069
19	39073481	39073482	C	A	14	GENIC	homozygous	109816071
19	39073705	39073706	T	C	18	GENIC	homozygous	109816073
19	39073885	39073886	A	C	21	GENIC	homozygous	109816076
19	39073925	39073926	C	T	22	GENIC	homozygous	109816078
19	39073928	39073929	T	C	21	GENIC	homozygous	109816080
19	39074008	39074009	A	G	27	GENIC	homozygous	109816082
19	39074112	39074113	A	G	27	GENIC	homozygous	109816084
19	39074193	39074194	T	G	27	GENIC	homozygous	109816086
19	39074340	39074341	A	G	19	GENIC	homozygous	109816088
19	39074414	39074415	A	C	21	GENIC	homozygous	109816090
19	39074452	39074453	A	G	28	GENIC	homozygous	109816092
19	39074479	39074480	C	T	27	GENIC	homozygous	109816094
19	39077469	39077470	G	A	27	GENIC	homozygous	109816096