chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
19	62869681	62869682	A	G	28	GENIC	homozygous	46729310
19	62869790	62869791	C	A	22	GENIC	possibly homozygous	46310569
19	62869967	62869968	A	G	19	GENIC	homozygous	46729312
19	62869973	62869974	G	A	19	GENIC	possibly homozygous	46729314
19	62870437	62870438	C	T	17	GENIC	homozygous	46310571
19	62870874	62870875	C	T	19	GENIC	homozygous	46729316
19	62870899	62870900	T	C	14	GENIC	homozygous	46729317
19	62871256	62871257	T	TA	17	GENIC	homozygous	46729319
19	62871837	62871838	A	C	49	GENIC	possibly homozygous	46729321
19	62876192	62876193	C	T	32	GENIC	possibly homozygous	46729323
19	62877575	62877576	T	TA	12	GENIC	possibly homozygous	46520875
19	62879594	62879595	G	GC	17	GENIC	homozygous	46183487
19	62879815	62879816	C	T	29	GENIC	possibly homozygous	46729325
19	62879858	62879859	G	A	25	GENIC	possibly homozygous	46729327
19	62880004	62880005	C	A	29	GENIC	possibly homozygous	46310602
19	62885206	62885208	AA	--	14	GENIC	heterozygous	46685897
19	62885789	62885790	G	GGT	1	GENIC	homozygous	46729329
19	62885896	62885897	C	T	20	GENIC	possibly homozygous	46729331
19	62885975	62885976	T	C	35	GENIC	homozygous	46729333
19	62887623	62887624	A	T	22	GENIC	possibly homozygous	46310634
19	62887700	62887701	C	T	32	GENIC	homozygous	46729335
19	62888150	62888151	C	T	26	GENIC	possibly homozygous	46310635
19	62888540	62888541	C	T	20	GENIC	homozygous	46310636