chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
16	81155426	81155427	A	AC	2	GENIC	homozygous	47565456
16	81155869	81155870	A	AAC	2	GENIC	homozygous	47565458
16	81156006	81156007	C	CT	3	GENIC	heterozygous	47565459
16	81157845	81157846	A	G	15	GENIC	homozygous	47565461
16	81158053	81158054	C	T	22	GENIC	homozygous	47565463
16	81159462	81159463	G	GTT	1	GENIC	homozygous	47565465
16	81159606	81159608	TG	--	3	GENIC	homozygous	47565467
16	81159999	81160000	T	C	10	GENIC	possibly homozygous	47565469
16	81160009	81160010	G	GTCTCTCTCTCTCTCTCTC	1	GENIC	homozygous	47997963
16	81160273	81160274	A	AT	9	GENIC	possibly homozygous	47565471
16	81160476	81160477	G	C	19	GENIC	homozygous	47565473
16	81160911	81160912	C	T	1	GENIC	homozygous	47565475
16	81160940	81160941	G	T	1	GENIC	homozygous	47565485
16	81161166	81161167	A	G	10	GENIC	homozygous	47565487
16	81161695	81161696	G	A	12	GENIC	heterozygous	47565488
16	81161705	81161706	A	C	9	GENIC	possibly homozygous	47565490
16	81162013	81162014	T	C	22	GENIC	homozygous	47565492
16	81162713	81162714	G	A	17	GENIC	possibly homozygous	47565494
16	81164927	81164928	G	A	19	GENIC	possibly homozygous	47565500
16	81165380	81165381	C	T	13	GENIC	homozygous	47565502
16	81168324	81168325	C	-	16	GENIC	possibly homozygous	47565503
16	81168864	81168865	A	AG	4	GENIC	homozygous	47565505