chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
10	36481102	36481103	T	C	22	GENIC	homozygous	52139453
10	36481330	36481331	G	A	19	GENIC	homozygous	52139455
10	36482343	36482344	G	A	28	GENIC	homozygous	52139457
10	36483590	36483591	T	-	21	GENIC	homozygous	51414335
10	36483876	36483877	T	C	21	GENIC	homozygous	52139459
10	36484069	36484070	C	CA	30	GENIC	homozygous	52139461
10	36484685	36484686	T	C	31	GENIC	homozygous	52139463
10	36484938	36484939	C	T	24	GENIC	homozygous	52139465
10	36485184	36485185	A	G	21	GENIC	homozygous	52139467
10	36485634	36485636	TC	--	22	GENIC	homozygous	52139469
10	36485769	36485770	A	-	21	GENIC	homozygous	52139471
10	36485894	36485895	A	C	21	GENIC	homozygous	52139473
10	36485969	36485973	TGAA	----	25	GENIC	homozygous	52040550
10	36486116	36486117	A	T	23	GENIC	homozygous	52139475
10	36486151	36486152	T	C	17	GENIC	homozygous	52139477
10	36486617	36486618	G	C	32	GENIC	homozygous	52139479
10	36487692	36487693	T	TA	26	GENIC	possibly homozygous	52139481
10	36487693	36487694	A	-	26	GENIC	heterozygous	52040552
10	36487948	36487949	G	T	22	GENIC	homozygous	51414343
10	36488188	36488189	C	T	17	GENIC	homozygous	52139483
10	36488212	36488213	T	C	15	GENIC	homozygous	52139485
10	36488259	36488260	T	C	10	GENIC	homozygous	51414345
10	36488775	36488776	C	A	4	GENIC	homozygous	51414347