chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
1	60885073	60885074	A	T	20	GENIC	homozygous	108121330
1	60885476	60885477	T	G	29	GENIC	homozygous	108121331
1	60886814	60886815	T	C	22	GENIC	homozygous	108121332
1	60887081	60887082	C	G	31	GENIC	homozygous	108121333
1	60887516	60887517	A	T	31	GENIC	homozygous	108121334
1	60887592	60887593	A	T	17	GENIC	homozygous	108121335
1	60887673	60887674	T	C	18	GENIC	homozygous	108121336
1	60888098	60888099	G	C	14	GENIC	homozygous	108121338
1	60888957	60888958	T	C	18	GENIC	homozygous	108121339
1	60889064	60889065	T	A	16	GENIC	homozygous	108121340
1	60889406	60889407	G	A	18	GENIC	homozygous	108121341
1	60889415	60889416	G	C	19	GENIC	homozygous	108121342
1	60889661	60889662	T	C	22	GENIC	possibly homozygous	108121343
1	60890118	60890119	A	G	20	GENIC	homozygous	108121344
1	60890223	60890224	G	A	22	GENIC	homozygous	108121345
1	60890463	60890464	G	T	28	GENIC	homozygous	108121346
1	60891210	60891211	T	C	24	GENIC	homozygous	108121347
1	60892688	60892689	G	A	28	GENIC	homozygous	108121348
1	60892809	60892810	T	G	20	GENIC	homozygous	108121349