chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
10	14005833	14005834	A	G	60	GENIC	possibly homozygous	51622556
10	14007903	14007904	C	T	63	GENIC	homozygous	51622557
10	14008199	14008200	A	G	41	GENIC	possibly homozygous	51622558
10	14008443	14008444	A	C	47	GENIC	homozygous	51622559
10	14008631	14008632	T	C	82	GENIC	possibly homozygous	51622560
10	14008807	14008808	G	A	76	GENIC	homozygous	51622561
10	14010708	14010709	G	GACAC	8	GENIC	heterozygous	51622562
10	14010708	14010709	G	GACACAC	8	GENIC	heterozygous	51622563
10	14012611	14012612	C	T	22	GENIC	homozygous	51622564
10	14012965	14012966	A	G	75	GENIC	homozygous	51622565
10	14013561	14013562	G	-	36	GENIC	heterozygous	51622566
10	14013562	14013563	G	T	47	GENIC	possibly homozygous	51622567
10	14013564	14013568	TTTG	----	35	GENIC	heterozygous	51622568
10	14013865	14013866	T	C	38	GENIC	homozygous	51622569
10	14013945	14013946	T	C	45	GENIC	homozygous	51622570
10	14014139	14014140	A	AT	42	GENIC	homozygous	51622571
10	14014220	14014221	A	T	20	GENIC	homozygous	51622572
10	14014236	14014237	A	ATTTT	1	GENIC	homozygous	51622573
10	14014801	14014802	T	TA	34	GENIC	homozygous	51622574
10	14014802	14014803	T	A	38	GENIC	homozygous	51622575
10	14014907	14014908	G	A	56	GENIC	homozygous	51622576