chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
10	59306517	59306518	A	C	4	GENIC	heterozygous	51465293
10	59306518	59306519	T	TA	4	GENIC	heterozygous	51465294
10	59308262	59308263	T	-	7	GENIC	homozygous	51465302
10	59308366	59308367	A	T	2	GENIC	heterozygous	51662937
10	59309038	59309039	G	A	15	GENIC	homozygous	51465306
10	59309136	59309137	C	T	20	GENIC	possibly homozygous	51465307
10	59310029	59310030	C	A	26	GENIC	homozygous	51465308
10	59310380	59310381	A	G	23	GENIC	possibly homozygous	51465310
10	59310717	59310718	T	C	15	GENIC	homozygous	51465311
10	59310868	59310869	C	T	16	GENIC	homozygous	51465312
10	59311552	59311553	C	G	5	GENIC	homozygous	51465314
10	59311924	59311925	C	T	9	GENIC	homozygous	51465316
10	59312489	59312490	G	A	15	GENIC	homozygous	51465317
10	59312928	59312929	T	C	11	GENIC	homozygous	51465318
10	59313114	59313115	T	C	18	GENIC	possibly homozygous	51465319
10	59313531	59313532	T	C	16	GENIC	homozygous	51465320
10	59314557	59314558	G	A	4	GENIC	heterozygous	51465321
10	59314949	59314950	A	G	16	GENIC	homozygous	51465322
10	59315564	59315565	T	C	13	GENIC	homozygous	51897422
10	59317242	59317243	C	-	19	GENIC	homozygous	52062159
10	59320139	59320140	G	A	15	GENIC	possibly homozygous	52062161