chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
19	630982	630983	A	C	13	GENIC	possibly homozygous	46206407
19	631554	631555	T	G	32	GENIC	homozygous	46206408
19	631843	631844	C	T	18	GENIC	homozygous	46206409
19	632344	632345	C	T	9	GENIC	homozygous	46206410
19	632714	632715	T	TGG	2	GENIC	homozygous	46206411
19	632775	632776	T	C	7	GENIC	homozygous	46206412
19	633623	633624	T	C	22	GENIC	possibly homozygous	46206414
19	633822	633823	G	A	1	GENIC	homozygous	46206415
19	633824	633825	G	T	1	GENIC	homozygous	46206416
19	634519	634520	C	A	25	GENIC	heterozygous	46206417
19	634776	634777	G	C	10	GENIC	homozygous	46206418
19	635204	635205	T	C	16	GENIC	possibly homozygous	46206419
19	635317	635318	C	CT	4	GENIC	heterozygous	46206420
19	635516	635518	AA	--	4	GENIC	homozygous	46206421
19	635624	635625	C	T	17	GENIC	homozygous	46206422
19	636201	636202	C	T	24	GENIC	homozygous	46206423
19	637039	637040	G	A	11	GENIC	heterozygous	46206424
19	637613	637615	TA	--	6	GENIC	homozygous	46206425
19	638841	638842	A	G	13	GENIC	possibly homozygous	46206426
19	638953	638954	G	C	16	GENIC	homozygous	46206427
19	639201	639202	G	-	7	GENIC	homozygous	46206428
19	639711	639712	A	C	2	GENIC	heterozygous	46040479
19	639712	639713	G	T	2	GENIC	heterozygous	46040481