chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
16	32460779	32460780	T	A	23	GENIC	homozygous	111959108
16	32460787	32460788	A	T	24	GENIC	homozygous	111959110
16	32460796	32460797	A		22	GENIC	homozygous	129350437
16	32460797	32460798	T	C	22	GENIC	homozygous	111781467
16	32460802	32460803	T	A	24	GENIC	homozygous	111959112
16	32460809	32460810	T	A	25	GENIC	homozygous	111959114
16	32460811	32460812	G	C	25	GENIC	homozygous	111959116
16	32460814	32460815	T	C	25	GENIC	homozygous	111959118
16	32461209	32461209		TGCTTGCTAGGCAAGCGCTCTACCACTGAGCTAAATCCCCA	15	GENIC	homozygous	129350438
16	32486775	32486776	G	T	29	GENIC	homozygous	111781469
16	32486779	32486780	G	A	29	GENIC	homozygous	111781471
16	32486799	32486800	G		28	GENIC	homozygous	129350439
16	32486813	32486813		A	26	GENIC	homozygous	129350440
16	32486850	32486851	A		25	GENIC	homozygous	129350441
16	32486883	32486884	G		23	GENIC	homozygous	129350442
16	32486893	32486894	C		24	GENIC	homozygous	129350443
16	32486900	32486901	C		25	GENIC	homozygous	129350444
16	32486938	32486939	C	T	23	GENIC	homozygous	111959122
16	32486939	32486940	A	C	23	GENIC	homozygous	111959124
16	32486966	32486967	A		22	GENIC	homozygous	129350445
16	32486989	32486990	T		21	GENIC	homozygous	129350446
16	32487002	32487003	A	T	22	GENIC	homozygous	111781473
16	32487003	32487004	T	A	22	GENIC	homozygous	111959126
16	32487007	32487008	T	A	20	GENIC	homozygous	111959128
16	32487012	32487013	G		19	GENIC	homozygous	129350447
16	32487017	32487017		G	20	GENIC	homozygous	129350448
16	32487020	32487020		A	19	GENIC	homozygous	129350449
16	32487086	32487086		A	18	GENIC	homozygous	129350450
16	32487087	32487087		C	18	GENIC	homozygous	129350451
16	32487105	32487106	G	A	18	GENIC	homozygous	111959130
16	32508745	32508745		G	26	GENIC	homozygous	129350452
16	32509244	32509245	G	A	25	GENIC	heterozygous	124204661
16	32509693	32509694	T	C	27	GENIC	heterozygous	119112018