chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
10	56001168	56001168		A	13	GENIC	possibly homozygous	130392704
10	56001646	56001647	T		21	GENIC	homozygous	131094408
10	56008661	56008662	G	C	8	GENIC	homozygous	123362779
10	56008776	56008777	G	C	22	GENIC	homozygous	116602950
10	56008557	56008558	A	G	20	GENIC	homozygous	116602946
10	56008560	56008561	G	C	19	GENIC	homozygous	116602948
10	56008621	56008621		T	13	GENIC	homozygous	128819073
10	56008626	56008627	C		13	GENIC	homozygous	128819074
10	56008663	56008668	GTGGC		8	GENIC	homozygous	128819075
10	56008677	56008677		GT	9	GENIC	homozygous	128819076
10	56008717	56008717		G	12	GENIC	homozygous	128819077
10	56008736	56008737	C		16	GENIC	homozygous	128819078
10	56008680	56008681	T	G	10	GENIC	homozygous	116978038
10	56008823	56008823		C	24	GENIC	homozygous	128819079
10	56008850	56008850		T	25	GENIC	homozygous	128819080
10	56008886	56008887	A		25	GENIC	homozygous	128819081
10	56008897	56008899	AG		24	GENIC	homozygous	128819082