chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
10	73520852	73520852		T	22	GENIC	heterozygous	130682034
10	73537861	73537861		A	45	GENIC	homozygous	128830433
10	73551508	73551508		CAA	30	GENIC	homozygous	128830436
10	73552086	73552087	C	T	13	GENIC	heterozygous	131711935
10	73555998	73555999	C	T	14	GENIC	homozygous	118001183
10	73558389	73558390	A	C	28	GENIC	heterozygous	131711938
10	73558388	73558389	A	C	25	GENIC	heterozygous	116800104
10	73558395	73558396	A	C	29	GENIC	heterozygous	116800106
10	73558396	73558397	A	C	30	GENIC	heterozygous	131101804
10	73574614	73574615	C	A	30	GENIC	possibly homozygous	116800108
10	73608770	73608771	C		3	GENIC	homozygous	128830460
10	73608780	73608780		AT	4	GENIC	homozygous	128830461
10	73608822	73608823	C		7	GENIC	homozygous	128830462
10	73608827	73608828	T		8	GENIC	homozygous	128830463
10	73608836	73608837	A		10	GENIC	homozygous	128830464
10	73608862	73608863	C		12	GENIC	homozygous	130682035
10	73627825	73627826	A	G	45	GENIC	homozygous	116635347
10	73631036	73631037	G	C	38	GENIC	homozygous	117016600
10	73631039	73631040	A	C	38	GENIC	homozygous	117016601
10	73631040	73631041	A	C	38	GENIC	homozygous	117016602
10	73631042	73631043	A	G	39	GENIC	homozygous	117064133
10	73631083	73631084	C	G	38	GENIC	homozygous	117016603
10	73631088	73631089	C		38	GENIC	homozygous	128830475
10	73631091	73631092	C	A	36	GENIC	homozygous	117016604
10	73631094	73631095	T	G	37	GENIC	homozygous	117016605
10	73631098	73631099	T	G	38	GENIC	homozygous	117016606
10	73631100	73631101	G	C	38	GENIC	homozygous	117016607
10	73631109	73631110	T	C	40	GENIC	homozygous	117296436
10	73631111	73631112	A	C	40	GENIC	homozygous	117296438
10	73631114	73631115	G	C	40	GENIC	homozygous	117296440
10	73631038	73631039	A	C	38	GENIC	homozygous	116978925
10	73613363	73613364	A		51	GENIC	heterozygous	131466711