chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
10	14005833	14005834	A	G	21	GENIC	homozygous	51622556
10	14007903	14007904	C	T	25	GENIC	homozygous	51622557
10	14008199	14008200	A	G	20	GENIC	homozygous	51622558
10	14008443	14008444	A	C	18	GENIC	homozygous	51622559
10	14008631	14008632	T	C	20	GENIC	homozygous	51622560
10	14008807	14008808	G	A	21	GENIC	homozygous	51622561
10	14010708	14010709	G	GACAC	14	GENIC	heterozygous	51622562
10	14010708	14010709	G	GACACAC	14	GENIC	possibly homozygous	51622563
10	14012611	14012612	C	T	20	GENIC	homozygous	51622564
10	14012965	14012966	A	G	28	GENIC	homozygous	51622565
10	14013561	14013562	G	-	24	GENIC	homozygous	51622566
10	14013564	14013568	TTTG	----	24	GENIC	homozygous	51622568
10	14013865	14013866	T	C	17	GENIC	homozygous	51622569
10	14013945	14013946	T	C	18	GENIC	homozygous	51622570
10	14014139	14014140	A	AT	11	GENIC	homozygous	51622571
10	14014220	14014221	A	T	10	GENIC	homozygous	51622572
10	14014801	14014802	T	TA	22	GENIC	homozygous	51622574
10	14014802	14014803	T	A	24	GENIC	homozygous	51622575
10	14014907	14014908	G	A	22	GENIC	homozygous	51622576
10	14014236	14014237	A	ATTTTT	15	GENIC	homozygous	52481268