chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
16	50339643	50339644	T	C	25	GENIC	possibly homozygous	111815148
16	50339845	50339846	T	C	29	GENIC	possibly homozygous	111815152
16	50340119	50340120	C	T	14	GENIC	homozygous	111815154
16	50340255	50340256	C	T	26	GENIC	homozygous	111815156
16	50340324	50340325	A	G	28	GENIC	possibly homozygous	111815158
16	50340354	50340355	C	T	29	GENIC	possibly homozygous	112409993
16	50341064	50341065	A	G	26	GENIC	possibly homozygous	111815160
16	50341388	50341389	A	G	31	GENIC	possibly homozygous	112061351
16	50341580	50341581	T	C	27	GENIC	homozygous	111815164
16	50341716	50341717	C	G	29	GENIC	homozygous	111815166
16	50341936	50341937	T	C	26	GENIC	homozygous	112061352
16	50342398	50342399	G	T	20	GENIC	possibly homozygous	112061353
16	50342935	50342936	T	C	18	GENIC	homozygous	112210141
16	50343291	50343292	C	G	25	GENIC	possibly homozygous	111815172
16	50343628	50343629	G	A	24	GENIC	possibly homozygous	112061355
16	50344092	50344093	C	T	19	GENIC	possibly homozygous	112061356
16	50345005	50345006	A	G	18	GENIC	homozygous	111815188
16	50343018	50343019	G	C	20	GENIC	homozygous	112111648
16	50343022	50343023	G	C	20	GENIC	homozygous	112111650
16	50343027	50343028	A	T	20	GENIC	homozygous	112111652
16	50345340	50345341	A	T	20	GENIC	homozygous	112061358
16	50346239	50346240	T	C	13	GENIC	homozygous	112061359
16	50346240	50346241	C	A	14	GENIC	homozygous	112061360
16	50346242	50346243	T	G	14	GENIC	homozygous	111815194
16	50348245	50348246	G	A	26	GENIC	possibly homozygous	112409995
16	50348471	50348472	G	A	36	GENIC	possibly homozygous	112061365
16	50349652	50349653	T	C	26	GENIC	homozygous	111815224
16	50349653	50349654	C	T	26	GENIC	homozygous	111815226
16	50349718	50349719	T	G	19	GENIC	homozygous	111815228
16	50349735	50349736	G	A	16	GENIC	homozygous	111815230
16	50350272	50350273	A	G	35	GENIC	homozygous	111815242
16	50355051	50355052	G	A	22	GENIC	possibly homozygous	112409997
16	50358247	50358248	T	C	30	GENIC	possibly homozygous	111815291