chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
10	70872526	70872527	G	-	19	GENIC	possibly homozygous	51689606
10	70872526	70872527	G	GT	19	GENIC	possibly homozygous	51689608
10	70872804	70872805	A	G	27	GENIC	homozygous	51489542
10	70872838	70872839	C	CT	24	GENIC	homozygous	51689610
10	70873875	70873876	A	G	27	GENIC	homozygous	51489543
10	70873878	70873879	T	C	28	GENIC	homozygous	51489544
10	70874398	70874399	C	A	23	GENIC	homozygous	51689612
10	70874538	70874539	G	-	26	GENIC	homozygous	51689614
10	70874976	70874977	A	G	22	GENIC	homozygous	51489546
10	70875191	70875192	G	GTTT	3	GENIC	homozygous	51489548
10	70875293	70875294	C	T	17	GENIC	possibly homozygous	51689616
10	70875295	70875296	G	A	15	GENIC	homozygous	51689618
10	70875401	70875402	A	G	10	GENIC	homozygous	51489550
10	70876166	70876167	G	A	33	GENIC	homozygous	51689620
10	70876307	70876308	A	G	21	GENIC	homozygous	51489555
10	70876377	70876378	C	CAGG	43	GENIC	homozygous	51489556
10	70876588	70876589	T	A	38	GENIC	homozygous	51489557
10	70876791	70876792	A	AG	18	GENIC	homozygous	51489558
10	70877217	70877218	A	G	27	GENIC	homozygous	51689622
10	70877279	70877280	G	A	36	GENIC	homozygous	51489559
10	70877707	70877708	A	T	37	GENIC	homozygous	51689624
10	70878356	70878357	G	GA	19	GENIC	possibly homozygous	51689626
10	70879288	70879289	A	C	24	GENIC	homozygous	51689628
10	70880138	70880140	AA	--	1	GENIC	homozygous	51489566
10	70880161	70880162	A	G	22	GENIC	homozygous	51489567
10	70880798	70880799	G	A	48	GENIC	homozygous	51689630
10	70883499	70883501	AA	--	13	GENIC	homozygous	51689632
10	70883695	70883696	T	G	19	GENIC	homozygous	51689634
10	70885310	70885311	T	C	15	GENIC	homozygous	51689636
10	70885843	70885850	TTGTGTC	-------	38	GENIC	heterozygous	51489574
10	70885843	70885844	T	TG	38	GENIC	homozygous	51489575
10	70885844	70885845	T	-	38	GENIC	heterozygous	51689638