chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
19	60299864	60299865	T	A	17	GENIC	homozygous	46178839
19	60299868	60299869	T	C	18	GENIC	homozygous	46178840
19	60299882	60299883	C	G	16	GENIC	homozygous	46178841
19	60299887	60299888	C	T	14	GENIC	homozygous	46178842
19	60299889	60299890	C	G	14	GENIC	homozygous	46178843
19	60299891	60299892	C	-	13	GENIC	homozygous	46178844
19	60299896	60299897	C	G	13	GENIC	homozygous	46178847
19	60299898	60299899	C	T	14	GENIC	homozygous	46178848
19	60302579	60302582	TGA	---	2	GENIC	homozygous	46178853
19	60307216	60307217	T	G	22	GENIC	homozygous	46178858
19	60307256	60307257	G	-	8	GENIC	homozygous	46178859
19	60307272	60307274	CA	--	7	GENIC	homozygous	46178860
19	60307277	60307278	G	T	8	GENIC	possibly homozygous	46178861
19	60307282	60307283	A	-	5	GENIC	homozygous	46178862
19	60307283	60307284	A	G	8	GENIC	heterozygous	46266877
19	60307291	60307292	T	TG	6	GENIC	homozygous	46178863
19	60307296	60307297	A	-	5	GENIC	homozygous	46178864
19	60307316	60307317	C	-	10	GENIC	homozygous	46178865
19	60307316	60307317	C	CA	10	GENIC	homozygous	46178866
19	60307322	60307323	T	-	12	GENIC	homozygous	46178867
19	60307326	60307327	C	-	9	GENIC	homozygous	46178868
19	60307326	60307327	C	CA	12	GENIC	heterozygous	46178869