chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
19	41630252	41630253	A	G	33	GENIC	homozygous	109702232
19	41630482	41630483	G	C	32	GENIC	possibly homozygous	109962099
19	41631353	41631354	T	A	31	GENIC	homozygous	110123354
19	41632333	41632334	C	T	32	GENIC	homozygous	109702234
19	41632690	41632691	G	C	9	GENIC	homozygous	109782156
19	41634188	41634189	C	T	39	GENIC	homozygous	109702236
19	41634511	41634512	C	A	45	GENIC	homozygous	109702238
19	41636139	41636140	T	C	34	GENIC	heterozygous	119630001
19	41636186	41636187	G	A	14	GENIC	homozygous	109702240
19	41636451	41636452	G	C	22	GENIC	homozygous	109702242
19	41636497	41636498	G	C	18	GENIC	homozygous	109702244
19	41636681	41636682	T	C	28	GENIC	homozygous	109702246
19	41637327	41637328	A	G	10	GENIC	homozygous	109702248
19	41637558	41637559	T	C	30	GENIC	homozygous	109702250
19	41637962	41637963	C	T	26	GENIC	homozygous	109702252
19	41639800	41639801	T	G	23	GENIC	homozygous	109702254
19	41639826	41639827	A	G	20	GENIC	homozygous	109782166
19	41641159	41641160	C	A	31	GENIC	homozygous	109702256
19	41636173	41636174	C	T	8	GENIC	homozygous	119630002