chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
10	75196099	75196100	G	-	8	GENIC	possibly homozygous	51498034
10	75197014	75197015	T	C	11	GENIC	possibly homozygous	51498035
10	75197442	75197443	T	C	12	GENIC	heterozygous	51498036
10	75198864	75198865	A	G	10	GENIC	possibly homozygous	52255383
10	75201108	75201109	C	T	19	GENIC	homozygous	52255385
10	75206897	75206909	AGTGGCAGTGGC	------------	1	GENIC	homozygous	52386228
10	75207811	75207812	T	C	6	GENIC	homozygous	52255389
10	75208160	75208161	A	G	4	GENIC	heterozygous	51498040
10	75208176	75208177	T	C	4	GENIC	heterozygous	51498041
10	75209305	75209306	T	C	22	GENIC	possibly homozygous	52255391
10	75210385	75210386	T	C	20	GENIC	homozygous	52255393
10	75210957	75210958	G	C	8	GENIC	possibly homozygous	52255395
10	75211099	75211100	G	A	15	GENIC	homozygous	52255397
10	75211670	75211671	A	AGG	1	GENIC	homozygous	52255399
10	75212070	75212072	AG	--	4	GENIC	heterozygous	52255401
10	75212193	75212194	G	A	6	GENIC	homozygous	52255403
10	75212838	75212839	C	CCA	12	GENIC	homozygous	51498044
10	75213075	75213076	A	AT	2	GENIC	homozygous	52255407
10	75213092	75213093	G	C	1	GENIC	homozygous	52255409