chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
10	90435695	90435699	AAAA	----	5	GENIC	heterozygous	51928235
10	90435696	90435699	AAA	---	5	GENIC	heterozygous	51538455
10	90436829	90436830	A	G	22	GENIC	homozygous	51538456
10	90437092	90437093	T	TA	5	GENIC	homozygous	51736653
10	90437440	90437441	G	A	15	GENIC	homozygous	51736655
10	90437704	90437705	T	TA	16	GENIC	homozygous	51538457
10	90438268	90438269	C	-	9	GENIC	homozygous	51736657
10	90438516	90438517	G	T	22	GENIC	homozygous	51736659
10	90440626	90440627	T	A	20	GENIC	homozygous	51538459
10	90441205	90441206	G	A	19	GENIC	homozygous	51736661
10	90441631	90441632	A	-	13	GENIC	heterozygous	51538460
10	90442024	90442025	T	C	14	GENIC	homozygous	51538461
10	90442743	90442744	T	-	32	GENIC	homozygous	51538462
10	90442927	90442928	C	G	17	GENIC	homozygous	51538463
10	90444046	90444047	A	G	31	GENIC	homozygous	51736663
10	90444941	90444942	G	GAAAA	14	GENIC	heterozygous	51538465
10	90444941	90444942	G	GAAA	14	GENIC	possibly homozygous	51538466
10	90445052	90445053	T	C	23	GENIC	possibly homozygous	51538467
10	90445233	90445234	C	T	13	GENIC	homozygous	51538468
10	90445254	90445255	T	-	17	GENIC	homozygous	51538469
10	90445463	90445464	C	CAAA	4	GENIC	heterozygous	51538471
10	90445543	90445544	C	G	25	GENIC	homozygous	51538472
10	90446010	90446011	A	T	27	GENIC	homozygous	51538473
10	90446298	90446299	G	T	29	GENIC	possibly homozygous	51538474
10	90447000	90447001	A	G	16	GENIC	homozygous	51538475
10	90447001	90447002	C	T	16	GENIC	homozygous	51538476