chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
10	38561416	38561419	AGC	---	23	GENIC	possibly homozygous	52042984
10	38561796	38561797	C	T	31	GENIC	homozygous	52042986
10	38561937	38561938	A	G	40	GENIC	possibly homozygous	51853062
10	38562332	38562333	A	C	35	GENIC	possibly homozygous	51853065
10	38562374	38562375	C	G	14	GENIC	possibly homozygous	51853068
10	38562478	38562479	C	A	34	GENIC	possibly homozygous	51853071
10	38562721	38562725	GTGC	----	21	GENIC	possibly homozygous	51985044
10	38562825	38562826	T	C	13	GENIC	heterozygous	51853079
10	38562907	38562908	T	TTTTA	19	GENIC	homozygous	51853082
10	38562980	38562981	T	C	24	GENIC	possibly homozygous	51853084
10	38563072	38563073	C	T	25	GENIC	possibly homozygous	52042988
10	38563181	38563182	A	G	33	GENIC	possibly homozygous	51853087
10	38563236	38563237	A	C	21	GENIC	possibly homozygous	51853090
10	38563326	38563327	G	A	29	GENIC	homozygous	52042990
10	38563442	38563443	A	G	25	GENIC	homozygous	51853093
10	38563655	38563656	C	CAG	27	GENIC	possibly homozygous	52042992
10	38563829	38563830	C	T	17	GENIC	possibly homozygous	51853096
10	38563910	38563912	AA	--	17	GENIC	homozygous	51853100
10	38564212	38564213	A	AG	19	GENIC	heterozygous	52042994
10	38564243	38564244	C	G	16	GENIC	homozygous	52043000
10	38564385	38564386	A	G	22	GENIC	possibly homozygous	51853109
10	38564664	38564665	G	A	15	GENIC	homozygous	52043002
10	38564705	38564706	T	TC	14	GENIC	homozygous	51853112