chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
19	52991925	52991926	T	C	22	GENIC	homozygous	109788774
19	52992250	52992251	C	G	5	GENIC	homozygous	119632890
19	52992358	52992359	C	T	11	GENIC	homozygous	109788776
19	52996221	52996222	C	A	26	GENIC	homozygous	109730398
19	52998009	52998010	G	C	32	GENIC	homozygous	109730400
19	52998096	52998097	A	C	38	GENIC	homozygous	109730402
19	52998131	52998132	G	C	38	GENIC	homozygous	109730404
19	52998263	52998264	C	A	11	GENIC	homozygous	109730410
19	52998979	52998980	T	C	29	GENIC	homozygous	119632892
19	52999138	52999139	T	G	13	GENIC	homozygous	119646300
19	52999173	52999174	T	G	2	GENIC	homozygous	119646301
19	52999631	52999632	T	A	27	GENIC	homozygous	119632897
19	52999638	52999639	A	C	26	GENIC	homozygous	110066181
19	52999735	52999736	C	A	42	GENIC	homozygous	109939895
19	53000046	53000047	A	G	43	GENIC	homozygous	119632899
19	52996309	52996310	G	C	38	GENIC	homozygous	109825347
19	52999606	52999607	T	C	39	GENIC	homozygous	109963033
19	52998832	52998833	C	A	38	GENIC	homozygous	110014160
19	52999524	52999525	T	A	10	GENIC	homozygous	109987217