chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
17	80547343	80547344	A	AT	13	GENIC	homozygous	47200035
17	80547353	80547354	G	GT	13	GENIC	homozygous	47200036
17	80547409	80547410	A	-	7	GENIC	homozygous	47200038
17	80547826	80547827	G	T	23	GENIC	homozygous	47200039
17	80548223	80548224	T	C	23	GENIC	homozygous	47200040
17	80548517	80548518	C	T	26	GENIC	homozygous	47200041
17	80548826	80548827	C	A	23	GENIC	homozygous	47453686
17	80549169	80549170	A	G	7	GENIC	homozygous	47200042
17	80549172	80549173	G	A	8	GENIC	homozygous	47200043
17	80549272	80549273	T	C	22	GENIC	homozygous	47200044
17	80549469	80549470	T	C	22	GENIC	homozygous	47453688
17	80549914	80549915	A	AG	30	GENIC	homozygous	47453689
17	80550117	80550120	TTT	---	3	GENIC	heterozygous	47200046
17	80550118	80550120	TT	--	3	GENIC	heterozygous	47200047
17	80550138	80550139	G	T	11	GENIC	homozygous	47200048
17	80550974	80550975	C	T	35	GENIC	homozygous	47453691
17	80551626	80551627	A	C	22	GENIC	homozygous	47453693
17	80551637	80551638	G	A	23	GENIC	homozygous	47453695
17	80552169	80552170	C	CCT	14	GENIC	homozygous	47200051
17	80552276	80552277	A	G	23	GENIC	possibly homozygous	47200052
17	80552457	80552458	C	T	24	GENIC	homozygous	47200054
17	80553577	80553578	A	AAAC	23	GENIC	homozygous	47453697
17	80553584	80553585	C	-	25	GENIC	homozygous	47453699
17	80553584	80553585	C	CAAA	23	GENIC	homozygous	47453701
17	80553602	80553603	A	C	25	GENIC	possibly homozygous	47453703
17	80553616	80553617	C	A	23	GENIC	possibly homozygous	47453705
17	80553840	80553841	G	A	19	GENIC	homozygous	47453707
17	80554288	80554289	A	G	23	GENIC	homozygous	47200063
17	80553570	80553571	C	CAAA	16	GENIC	homozygous	47340488
17	80554347	80554348	T	TA	25	GENIC	homozygous	47200064
17	80554611	80554612	T	C	25	GENIC	homozygous	47453709
17	80554118	80554119	T	A	26	GENIC	homozygous	47340490