chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
10	70215143	70215144	C	T	23	GENIC	heterozygous	403636604
10	70215143	70215144	C		23	GENIC	heterozygous	403636605
10	70218197	70218198	A	T	48	GENIC	possibly homozygous	403938417
10	70218197	70218198	A		48	GENIC	heterozygous	403938418
10	70235516	70235517	G	A	72	GENIC	homozygous	138813968
10	70235831	70235832	G	C	28	GENIC	homozygous	138813969
10	70286292	70286293	G	A	46	GENIC	heterozygous	138814014
10	70328000	70328001	T	C	5	GENIC	heterozygous	403289569
10	70262600	70262603	TTT		36	GENIC	homozygous	138689640
10	70328000	70328001	T		5	GENIC	homozygous	403289570
10	70328004	70328005	T	C	5	GENIC	heterozygous	403289571
10	70328004	70328005	T		5	GENIC	homozygous	403289572
10	70327999	70328005	TTTCTT		5	GENIC	homozygous	141094874
10	70333606	70333607	C	T	62	GENIC	homozygous	138814037
10	70338298	70338299	G		17	GENIC	heterozygous	403636629
10	70338298	70338299	G	C	17	GENIC	heterozygous	403636630
10	70358643	70358644	A	C	15	GENIC	possibly homozygous	138814053
10	70358654	70358655	A	C	13	GENIC	heterozygous	141037890
10	70358654	70358655	A		13	GENIC	heterozygous	403289576
10	70369751	70369752	G		29	GENIC	heterozygous	403289579
10	70369751	70369752	G	C	29	GENIC	heterozygous	403289580
10	70421096	70421097	T		6	GENIC	heterozygous	403289581
10	70421096	70421097	T	G	6	GENIC	heterozygous	403289582
10	70429299	70429300	C	T	65	GENIC	possibly homozygous	143455230
10	70547864	70547865	C	G	77	GENIC	homozygous	143455231
10	70548621	70548622	T		12	GENIC	heterozygous	403636660
10	70548621	70548622	T	A	12	GENIC	heterozygous	403636661
10	70578556	70578557	G		21	GENIC	homozygous	138689734
10	70651258	70651258		C	22	GENIC	possibly homozygous	138689770
10	70557151	70557157	CTCTCT		5	GENIC	homozygous	149382958