chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
19	44165044	44165045	A	C	39	GENIC	homozygous	109709758
19	44165888	44165888		G	40	GENIC	homozygous	129611395
19	44167432	44167433	A	G	44	GENIC	homozygous	109784619
19	44167916	44167917	T	A	44	GENIC	homozygous	109784621
19	44168474	44168475	A	T	43	GENIC	homozygous	109709768
19	44168640	44168641	G	C	40	GENIC	homozygous	109784623
19	44169690	44169691	G	A	47	GENIC	homozygous	109709772
19	44169835	44169836	T	C	44	GENIC	homozygous	109709774
19	44170265	44170265		TC	38	GENIC	homozygous	129611399
19	44170993	44170999	GAAGTG		40	GENIC	homozygous	129611400
19	44172288	44172289	C	T	49	GENIC	homozygous	109709780
19	44172630	44172631	C	T	36	GENIC	homozygous	109709782
19	44173685	44173686	C	T	59	GENIC	homozygous	109709784
19	44173706	44173707	T	C	57	GENIC	homozygous	109709786
19	44168336	44168337	A	T	42	GENIC	homozygous	119630706
19	44168351	44168352	T	C	45	GENIC	homozygous	119630707
19	44168258	44168259	T	C	22	GENIC	homozygous	119665791
19	44168296	44168297	T	C	34	GENIC	homozygous	109929323
19	44169472	44169472		AATT	43	GENIC	homozygous	131219629
19	44175371	44175371		AT	26	GENIC	possibly homozygous	131219630
19	44175406	44175407	G	A	37	GENIC	homozygous	109784627
19	44173975	44173976	A	G	41	GENIC	homozygous	109709790
19	44174154	44174155	C	A	38	GENIC	homozygous	109709792
19	44174252	44174253	C	T	35	GENIC	homozygous	109709794
19	44174378	44174379	C	T	35	GENIC	homozygous	109784625
19	44175411	44175412	T	C	39	GENIC	homozygous	109709796