chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
19	630982	630983	A	C	15	GENIC	homozygous	46206407
19	631554	631555	T	G	12	GENIC	homozygous	46206408
19	631843	631844	C	T	16	GENIC	homozygous	46206409
19	632344	632345	C	T	13	GENIC	homozygous	46206410
19	632714	632715	T	TGG	12	GENIC	homozygous	46206411
19	632775	632776	T	C	15	GENIC	homozygous	46206412
19	633091	633092	G	GTC	2	GENIC	homozygous	46669380
19	633114	633115	A	-	20	GENIC	heterozygous	46579853
19	633117	633118	T	TG	11	GENIC	heterozygous	46669383
19	633120	633137	GGAATCAAACCTAGGGC	-----------------	15	GENIC	heterozygous	46669386
19	633623	633624	T	C	19	GENIC	homozygous	46206414
19	633822	633823	G	A	19	GENIC	homozygous	46206415
19	633824	633825	G	T	19	GENIC	homozygous	46206416
19	634519	634520	C	A	25	GENIC	homozygous	46206417
19	634776	634777	G	C	18	GENIC	homozygous	46206418
19	635204	635205	T	C	14	GENIC	homozygous	46206419
19	635317	635318	C	CT	12	GENIC	homozygous	46206420
19	635516	635518	AA	--	14	GENIC	possibly homozygous	46206421
19	635517	635518	A	-	14	GENIC	heterozygous	46040471
19	635624	635625	C	T	21	GENIC	homozygous	46206422
19	636201	636202	C	T	21	GENIC	homozygous	46206423
19	637039	637040	G	A	23	GENIC	homozygous	46206424
19	637613	637615	TA	--	14	GENIC	homozygous	46206425
19	638841	638842	A	G	13	GENIC	homozygous	46206426
19	638953	638954	G	C	16	GENIC	possibly homozygous	46206427
19	639201	639202	G	-	18	GENIC	homozygous	46206428
19	639341	639342	C	G	6	GENIC	homozygous	46040477
19	639711	639712	A	C	4	GENIC	homozygous	46040479
19	639712	639713	G	T	4	GENIC	homozygous	46040481
19	639736	639737	A	T	1	GENIC	homozygous	46040483
19	639728	639729	C	CTT	2	GENIC	homozygous	46394342
19	639731	639733	GA	--	2	GENIC	homozygous	46394345
19	639733	639734	A	T	2	GENIC	homozygous	46394348