chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
10	75253303	75253305	CA	--	10	GENIC	heterozygous	52461594
10	75262276	75262277	G	GT	12	GENIC	homozygous	51498117
10	75262288	75262289	A	AT	15	GENIC	homozygous	51498118
10	75262295	75262296	A	T	15	GENIC	homozygous	52321316
10	75262296	75262297	C	A	15	GENIC	homozygous	52321318
10	75271108	75271109	A	-	11	GENIC	heterozygous	52461596
10	75302926	75302927	C	-	19	GENIC	heterozygous	51697355
10	75309375	75309376	A	G	16	GENIC	homozygous	51498209
10	75310097	75310098	G	GTTT	1	GENIC	homozygous	52504524
10	75317251	75317252	T	TA	15	GENIC	homozygous	51498231
10	75319745	75319747	CA	--	8	GENIC	heterozygous	52461597
10	75322713	75322714	A	AG	4	GENIC	heterozygous	52386302
10	75331093	75331094	T	-	30	GENIC	heterozygous	51498264
10	75332603	75332604	G	A	23	GENIC	heterozygous	51498272
10	75332819	75332820	T	TC	1	GENIC	homozygous	51498275
10	75340635	75340636	G	GA	15	GENIC	heterozygous	51912494
10	75340636	75340637	A	-	15	GENIC	heterozygous	52321320
10	75344993	75344994	A	G	15	GENIC	homozygous	51498319
10	75346875	75346877	TT	--	13	GENIC	heterozygous	51498324
10	75353584	75353585	C	A	3	GENIC	homozygous	51498356
10	75353590	75353591	C	A	3	GENIC	homozygous	52386316
10	75355880	75355881	G	GA	7	GENIC	homozygous	51498363
10	75358700	75358701	G	-	18	GENIC	heterozygous	52386320
10	75368890	75368891	C	CT	5	GENIC	homozygous	51498402
10	75372002	75372003	T	-	11	GENIC	heterozygous	52461598
10	75372816	75372817	G	GA	23	GENIC	homozygous	51498412
10	75372818	75372819	A	T	24	GENIC	homozygous	51498413
10	75346876	75346877	T	-	13	GENIC	heterozygous	51988417