chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
10	48359039	48359040	G	A	17	GENIC	homozygous	52055441
10	48360091	48360092	A	G	45	GENIC	homozygous	51639309
10	48362166	48362167	C	T	20	GENIC	homozygous	51639313
10	48362587	48362588	A	-	20	GENIC	possibly homozygous	52055443
10	48362660	48362661	T	C	29	GENIC	homozygous	51639314
10	48363742	48363743	C	G	27	GENIC	homozygous	52055446
10	48364483	48364484	G	A	23	GENIC	homozygous	52055448
10	48365480	48365481	T	C	19	GENIC	homozygous	51639323
10	48365539	48365540	A	G	22	GENIC	homozygous	51639324
10	48367189	48367190	C	CA	6	GENIC	heterozygous	52318293
10	48368903	48368904	C	G	36	GENIC	homozygous	51639329
10	48369044	48369045	A	AT	25	GENIC	homozygous	51446988
10	48369330	48369331	G	T	30	GENIC	homozygous	51639330
10	48370046	48370047	C	T	28	GENIC	homozygous	52055450
10	48370065	48370066	T	C	30	GENIC	homozygous	52055452
10	48371276	48371277	C	T	20	GENIC	homozygous	51639334
10	48373103	48373104	G	GGTTTT	28	GENIC	homozygous	51639335
10	48373125	48373126	T	TTTG	22	GENIC	possibly homozygous	51639336
10	48373313	48373314	T	C	47	GENIC	homozygous	51639337
10	48373998	48373999	G	A	26	GENIC	homozygous	51639338