chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
19	44172630	44172631	C	T	26	GENIC	homozygous	109709782
19	44172854	44172855	C	T	44	GENIC	homozygous	109929327
19	44173685	44173686	C	T	35	GENIC	homozygous	109709784
19	44173706	44173707	T	C	39	GENIC	homozygous	109709786
19	44173887	44173888	G	A	32	GENIC	homozygous	109929329
19	44174154	44174155	C	A	32	GENIC	homozygous	109709792
19	44174252	44174253	C	T	23	GENIC	homozygous	109709794
19	44175411	44175412	T	C	28	GENIC	homozygous	109709796
19	44177113	44177114	A	T	32	GENIC	homozygous	109709798
19	44177114	44177115	A	C	32	GENIC	homozygous	109709800
19	44178719	44178720	T	C	24	GENIC	homozygous	109709804
19	44179923	44179924	A	T	45	GENIC	homozygous	109709806
19	44181198	44181199	C	T	35	GENIC	homozygous	109929331
19	44181986	44181987	C	T	12	GENIC	homozygous	109709808
19	44183417	44183418	A	C	31	GENIC	homozygous	109709810
19	44183882	44183883	G	A	22	GENIC	homozygous	109709812
19	44190366	44190367	C	T	31	GENIC	homozygous	109709814
19	44191845	44191846	G	T	31	GENIC	homozygous	109929333
19	44191979	44191980	G	A	26	GENIC	homozygous	109709816
19	44194698	44194699	C	A	17	GENIC	homozygous	109709820
19	44201065	44201066	A	C	30	GENIC	homozygous	109709822
19	44201144	44201145	C	T	39	GENIC	homozygous	109818653
19	44201166	44201167	G	A	42	GENIC	homozygous	109929335
19	44201260	44201261	G	T	33	GENIC	homozygous	109818655
19	44201291	44201292	G	A	27	GENIC	homozygous	109818657
19	44201295	44201296	C	A	25	GENIC	homozygous	109929337
19	44201359	44201360	C	G	29	GENIC	homozygous	109929339
19	44203048	44203049	C	T	25	GENIC	homozygous	109709840
19	44203989	44203990	A	G	37	GENIC	homozygous	109709868