chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
10	66304681	66304682	G	A	16	GENIC	possibly homozygous	51479477
10	66304726	66304727	T	-	5	GENIC	homozygous	51479478
10	66304915	66304916	A	AGTCTGTCT	6	GENIC	heterozygous	52996188
10	66304916	66304920	GTCT	----	6	GENIC	heterozygous	51479479
10	66304997	66304998	T	-	22	GENIC	homozygous	51479480
10	66305422	66305423	C	T	21	GENIC	possibly homozygous	52996190
10	66305908	66305909	G	A	20	GENIC	homozygous	52996192
10	66306014	66306015	C	T	14	GENIC	homozygous	52996194
10	66306467	66306468	T	C	23	GENIC	possibly homozygous	51479483
10	66307144	66307145	G	A	13	GENIC	homozygous	51479484
10	66307753	66307754	G	GC	6	GENIC	heterozygous	52996196
10	66308588	66308589	T	-	7	GENIC	possibly homozygous	52996198
10	66309171	66309172	C	T	36	GENIC	possibly homozygous	51479487
10	66310063	66310064	T	A	2	GENIC	homozygous	52996200
10	66310064	66310065	G	GA	2	GENIC	homozygous	52996203
10	66310065	66310066	T	TA	2	GENIC	homozygous	52996205
10	66310788	66310789	C	T	18	GENIC	possibly homozygous	52996207
10	66317257	66317258	A	-	1	GENIC	homozygous	52503847
10	66318225	66318226	G	T	32	GENIC	homozygous	52996209
10	66319044	66319045	G	-	19	GENIC	homozygous	51479494
10	66319598	66319599	C	T	20	GENIC	possibly homozygous	52996211
10	66319975	66319976	C	CA	11	GENIC	possibly homozygous	51479495
10	66322697	66322698	A	G	15	GENIC	homozygous	51479500
10	66324257	66324258	G	A	28	GENIC	possibly homozygous	52996213
10	66325748	66325749	A	-	4	GENIC	heterozygous	52996215
10	66325761	66325762	C	T	3	GENIC	heterozygous	51479509
10	66327047	66327048	A	G	15	GENIC	homozygous	51479512