chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
10	60282479	60282480	C	T	18	GENIC	homozygous	138801222
10	60282768	60282769	G	C	23	GENIC	homozygous	138801223
10	60283834	60283835	G	A	13	GENIC	homozygous	138801224
10	60286832	60286833	G	A	16	GENIC	homozygous	138801225
10	60287474	60287474		TTGT	14	GENIC	homozygous	138686238
10	60288633	60288634	A	T	17	GENIC	homozygous	138801226
10	60288954	60288954		CCTGGCCTGG	13	GENIC	homozygous	138686239
10	60290463	60290464	G	A	22	GENIC	homozygous	138801227
10	60291131	60291132	C	T	21	GENIC	homozygous	138801228
10	60291221	60291222	C	T	18	GENIC	homozygous	138801229
10	60292081	60292082	G	A	19	GENIC	homozygous	138801230
10	60292360	60292361	T	G	20	GENIC	homozygous	138801231
10	60292498	60292499	A	G	30	GENIC	homozygous	138801232
10	60293250	60293251	T	C	23	GENIC	homozygous	138801233
10	60294986	60294987	G	A	17	GENIC	homozygous	138801234
10	60295307	60295308	G	A	16	GENIC	homozygous	138801235