chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
19	44165044	44165045	A	C	44	GENIC	homozygous	109709758
19	44165888	44165888		G	48	GENIC	homozygous	129611395
19	44167432	44167433	A	G	56	GENIC	homozygous	109784619
19	44168068	44168069	A	G	26	GENIC	homozygous	131553311
19	44168090	44168212	AAGAAAGGTTTGTTTGTTTTTTTTTTTTTTTTTTATTAACTTGAGTATTTCTTATATACATTTCGAGTGTTATTCCCTTTCCCGGTTTCCGGGCAAACATCCCCCTCCCCCCTCCCCTTCCT		12	GENIC	homozygous	131550497
19	44168296	44168297	T	C	48	GENIC	homozygous	109929323
19	44168336	44168337	A	T	58	GENIC	homozygous	119630706
19	44168351	44168352	T	C	60	GENIC	homozygous	119630707
19	44168474	44168475	A	T	63	GENIC	homozygous	109709768
19	44169690	44169691	G	A	65	GENIC	homozygous	109709772
19	44169835	44169836	T	C	74	GENIC	homozygous	109709774
19	44170265	44170265		TC	46	GENIC	homozygous	129611399
19	44170993	44170999	GAAGTG		43	GENIC	homozygous	129611400
19	44171268	44171269	G	T	54	GENIC	homozygous	109929325
19	44172288	44172289	C	T	55	GENIC	homozygous	109709780
19	44172630	44172631	C	T	55	GENIC	homozygous	109709782
19	44172854	44172855	C	T	50	GENIC	homozygous	109929327
19	44173685	44173686	C	T	58	GENIC	homozygous	109709784
19	44173706	44173707	T	C	59	GENIC	homozygous	109709786
19	44173887	44173888	G	A	48	GENIC	homozygous	109929329
19	44173961	44173962	T	A	57	GENIC	homozygous	110081303
19	44173975	44173976	A	G	60	GENIC	homozygous	109709790
19	44174154	44174155	C	A	39	GENIC	homozygous	109709792
19	44174252	44174253	C	T	49	GENIC	homozygous	109709794
19	44175371	44175371		AT	55	GENIC	possibly homozygous	131219630
19	44175411	44175412	T	C	61	GENIC	homozygous	109709796