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	22	GENIC	homozygous	51498117
10	75262288	75262289	A	AT	20	GENIC	homozygous	51498118
10	75262295	75262296	A	T	20	GENIC	homozygous	52321316
10	75262296	75262297	C	A	20	GENIC	homozygous	52321318
10	75264621	75264622	T	TAC	2	GENIC	homozygous	53335856
10	75302926	75302927	C	-	9	GENIC	heterozygous	51697355
10	75309375	75309376	A	G	34	GENIC	homozygous	51498209
10	75310097	75310098	G	GTTT	3	GENIC	homozygous	52504524
10	75312265	75312267	AC	--	15	GENIC	heterozygous	51498214
10	75317251	75317252	T	TA	15	GENIC	homozygous	51498231
10	75328547	75328549	CG	--	17	GENIC	heterozygous	52442011
10	75331093	75331094	T	-	48	GENIC	heterozygous	51498264
10	75332603	75332604	G	A	60	GENIC	heterozygous	51498272
10	75332819	75332820	T	TC	2	GENIC	homozygous	51498275
10	75340635	75340636	G	GA	4	GENIC	heterozygous	51912494
10	75344154	75344155	C	CTTT	17	GENIC	heterozygous	51988414
10	75344155	75344156	T	-	17	GENIC	heterozygous	52846686
10	75344993	75344994	A	G	19	GENIC	possibly homozygous	51498319
10	75353584	75353585	C	A	14	GENIC	homozygous	51498356
10	75353590	75353591	C	A	11	GENIC	homozygous	52386316
10	75355880	75355881	G	GA	12	GENIC	homozygous	51498363
10	75358700	75358701	G	-	9	GENIC	heterozygous	52386320
10	75368890	75368891	C	CT	17	GENIC	homozygous	51498402
10	75372816	75372817	G	GA	17	GENIC	homozygous	51498412
10	75372818	75372819	A	T	16	GENIC	homozygous	51498413
10	75373859	75373861	TC	--	24	GENIC	heterozygous	52255851
10	75374098	75374100	AC	--	23	GENIC	heterozygous	52504526