chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
16	73198666	73198667	A	G	16	GENIC	homozygous	47520106
16	73199883	73199884	T	C	31	GENIC	homozygous	47520108
16	73199963	73199964	A	G	34	GENIC	homozygous	47520110
16	73200485	73200486	C	T	26	GENIC	possibly homozygous	47696008
16	73200788	73200789	C	T	27	GENIC	homozygous	47520111
16	73202279	73202280	T	G	28	GENIC	homozygous	47520116
16	73202702	73202703	G	A	28	GENIC	homozygous	47520117
16	73202904	73202905	G	A	14	GENIC	possibly homozygous	47696009
16	73203096	73203097	A	G	23	GENIC	possibly homozygous	47696010
16	73203099	73203100	G	A	25	GENIC	possibly homozygous	47935011
16	73204595	73204596	G	A	24	GENIC	homozygous	47520121
16	73205240	73205241	G	A	32	GENIC	possibly homozygous	47696011
16	73205317	73205318	G	A	28	GENIC	homozygous	47520122
16	73205393	73205394	C	T	29	GENIC	possibly homozygous	47696012
16	73205788	73205789	A	G	34	GENIC	homozygous	47520124
16	73205789	73205790	A	G	38	GENIC	homozygous	47520126
16	73206447	73206448	T	G	32	GENIC	homozygous	47520129
16	73206563	73206577	TGTTATTTCTCCAT	--------------	34	GENIC	homozygous	47696013
16	73206757	73206758	C	T	29	GENIC	homozygous	47520131
16	73206899	73206900	T	C	16	GENIC	homozygous	47520132
16	73206992	73206993	G	A	22	GENIC	homozygous	47520134
16	73207694	73207695	A	C	26	GENIC	homozygous	47520136
16	73207760	73207761	A	G	33	GENIC	homozygous	47520139
16	73207818	73207819	C	T	29	GENIC	possibly homozygous	47696014
16	73208233	73208234	G	A	34	GENIC	possibly homozygous	47520141
16	73208256	73208257	T	G	37	GENIC	homozygous	47520142
16	73209463	73209464	A	G	23	GENIC	homozygous	47520145
16	73209473	73209474	T	C	24	GENIC	homozygous	47520147
16	73210441	73210442	T	C	33	GENIC	homozygous	47520149
16	73211346	73211347	A	G	29	GENIC	homozygous	47520150
16	73211746	73211747	T	A	24	GENIC	homozygous	47520152
16	73212588	73212589	G	A	17	GENIC	homozygous	47520153
16	73212743	73212744	T	C	16	GENIC	homozygous	47520155
16	73213036	73213050	CAGCTCCGCCCCCC	--------------	6	GENIC	homozygous	47520158