chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
19	62734123	62734124	T	G	43	GENIC	homozygous	46310157
19	62734273	62734274	A	G	34	GENIC	homozygous	46310158
19	62734657	62734658	A	G	41	GENIC	heterozygous	46216259
19	62735111	62735112	C	G	31	GENIC	homozygous	46310159
19	62735518	62735519	G	A	32	GENIC	possibly homozygous	46310160
19	62735654	62735655	G	A	42	GENIC	homozygous	46310161
19	62735676	62735677	G	C	35	GENIC	possibly homozygous	46310162
19	62735711	62735712	C	T	31	GENIC	homozygous	46310163
19	62735822	62735824	TT	--	10	GENIC	heterozygous	46310164
19	62735831	62735832	T	G	12	GENIC	heterozygous	46310165
19	62735859	62735860	A	AGTTGAT	5	GENIC	homozygous	46310166
19	62736400	62736401	T	C	32	GENIC	homozygous	46310167
19	62736569	62736570	G	A	33	GENIC	homozygous	46310168
19	62736637	62736638	G	-	29	GENIC	homozygous	46310169
19	62736751	62736752	G	A	37	GENIC	homozygous	46310170
19	62737105	62737106	T	G	38	GENIC	homozygous	46310171
19	62737296	62737297	G	A	24	GENIC	possibly homozygous	46310172
19	62737555	62737556	A	G	29	GENIC	homozygous	46310173
19	62737833	62737834	G	A	38	GENIC	homozygous	46310174
19	62737844	62737845	T	A	38	GENIC	homozygous	46310175
19	62736055	62736056	C	CT	3	GENIC	homozygous	46183473