chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
8	50314090	50314091	A	G	25	GENIC	homozygous	116815509
8	50327542	50327543	T	C	10	GENIC	homozygous	116815511
8	50342358	50342359	T	C	15	GENIC	homozygous	116815513
8	50389702	50389703	T	A	23	GENIC	homozygous	116815531
8	50436651	50436652	T	C	19	GENIC	homozygous	116815535
8	50446194	50446195	G	C	20	GENIC	homozygous	117931276
8	50446195	50446196	C	A	20	GENIC	homozygous	117931277
8	50451293	50451294	C	T	31	GENIC	homozygous	116815539
8	50448030	50448031	T	C	14	GENIC	homozygous	116490266
8	50493489	50493490	A	G	17	GENIC	homozygous	116815545
8	50494166	50494167	C	T	30	GENIC	homozygous	116815547
8	50504913	50504914	T	C	19	GENIC	homozygous	116815549
8	50508585	50508586	A	G	29	GENIC	homozygous	116815551
8	50509032	50509033	A	C	18	GENIC	homozygous	117910336
8	50509138	50509139	A	C	29	GENIC	homozygous	116490272
8	50509163	50509164	G	C	30	GENIC	homozygous	116815553
8	50509570	50509571	T	C	22	GENIC	homozygous	117940873
8	50511358	50511359	T	C	32	GENIC	homozygous	116490278
8	50511399	50511400	A	T	28	GENIC	homozygous	117910339
8	50511400	50511401	A	C	28	GENIC	homozygous	117910340
8	50511575	50511576	G	A	39	GENIC	homozygous	117910341
8	50511576	50511577	A	G	36	GENIC	homozygous	117910342
8	50512339	50512340	C	G	31	GENIC	possibly homozygous	116815555
8	50513614	50513615	C	T	41	GENIC	homozygous	116815557
8	50513696	50513697	G	A	48	GENIC	homozygous	116815559
8	50515184	50515185	G	A	23	GENIC	homozygous	116815561
8	50515228	50515229	T	G	27	GENIC	homozygous	116815563
8	50516013	50516014	T	C	25	GENIC	homozygous	116815565
8	50516156	50516157	A	G	30	GENIC	homozygous	116815567
8	50516274	50516275	A	T	35	GENIC	homozygous	116815569
8	50519535	50519536	C	T	27	GENIC	homozygous	116815571