chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
8	50314090	50314091	A	G	21	GENIC	homozygous	116815509
8	50327542	50327543	T	C	27	GENIC	homozygous	116815511
8	50342358	50342359	T	C	28	GENIC	homozygous	116815513
8	50346144	50346145	G	T	21	GENIC	homozygous	117940872
8	50389702	50389703	T	A	28	GENIC	homozygous	116815531
8	50436651	50436652	T	C	22	GENIC	homozygous	116815535
8	50448030	50448031	T	C	24	GENIC	homozygous	116490266
8	50448497	50448498	T	A	40	GENIC	homozygous	116490268
8	50451293	50451294	C	T	31	GENIC	homozygous	116815539
8	50493489	50493490	A	G	22	GENIC	homozygous	116815545
8	50494166	50494167	C	T	30	GENIC	homozygous	116815547
8	50504913	50504914	T	C	33	GENIC	homozygous	116815549
8	50508585	50508586	A	G	38	GENIC	homozygous	116815551
8	50509138	50509139	A	C	24	GENIC	homozygous	116490272
8	50509163	50509164	G	C	25	GENIC	homozygous	116815553
8	50509283	50509284	G	A	16	GENIC	homozygous	117916783
8	50509284	50509285	A	G	16	GENIC	homozygous	117910337
8	50509570	50509571	T	C	27	GENIC	homozygous	117940873
8	50511358	50511359	T	C	22	GENIC	homozygous	116490278
8	50511399	50511400	A	T	29	GENIC	homozygous	117910339
8	50511575	50511576	G	A	28	GENIC	homozygous	117910341
8	50511576	50511577	A	G	27	GENIC	homozygous	117910342
8	50512339	50512340	C	G	30	GENIC	homozygous	116815555
8	50513614	50513615	C	T	35	GENIC	homozygous	116815557
8	50513696	50513697	G	A	28	GENIC	homozygous	116815559
8	50515184	50515185	G	A	29	GENIC	homozygous	116815561
8	50515228	50515229	T	G	29	GENIC	homozygous	116815563
8	50516013	50516014	T	C	27	GENIC	homozygous	116815565
8	50516156	50516157	A	G	25	GENIC	homozygous	116815567
8	50516274	50516275	A	T	26	GENIC	homozygous	116815569
8	50517633	50517634	G	C	40	GENIC	homozygous	117940874
8	50517885	50517886	T	G	30	GENIC	homozygous	117940875
8	50518509	50518510	G	A	28	GENIC	homozygous	117940876
8	50518892	50518893	C	T	34	GENIC	homozygous	117940877
8	50519508	50519509	A	T	15	GENIC	homozygous	117940878