chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
19	43907023	43907024	C	G	25	GENIC	homozygous	109708652
19	43907291	43907292	T	G	23	GENIC	homozygous	109784245
19	43907345	43907346	A	G	17	GENIC	homozygous	109708655
19	43907346	43907347	A	T	17	GENIC	homozygous	109708657
19	43907347	43907348	A	T	15	GENIC	homozygous	109708659
19	43907362	43907363	G	A	14	GENIC	homozygous	109708661
19	43908152	43908153	C	G	25	GENIC	homozygous	109708665
19	43908167	43908168	T	C	25	GENIC	homozygous	109708667
19	43908217	43908218	G	C	36	GENIC	homozygous	109708669
19	43908242	43908243	G	A	36	GENIC	homozygous	109708671
19	43908247	43908248	G	A	38	GENIC	homozygous	109784247
19	43908672	43908673	A	C	42	GENIC	homozygous	109784249
19	43909220	43909221	A	T	22	GENIC	homozygous	109784251
19	43909285	43909286	C	T	26	GENIC	homozygous	109784253
19	43909331	43909332	G	A	33	GENIC	homozygous	109784255
19	43909535	43909536	C	A	33	GENIC	homozygous	109784257
19	43909800	43909801	C	T	28	GENIC	homozygous	109784259
19	43909957	43909958	T	G	30	GENIC	homozygous	109708679
19	43909958	43909959	T	G	28	GENIC	homozygous	109784261
19	43910774	43910775	G	T	42	GENIC	homozygous	109708689
19	43911002	43911003	G	C	45	GENIC	homozygous	109708693