chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
12	17344191	17344192	G	T	21	GENIC	possibly homozygous	115365079
12	17344263	17344264	C	G	24	GENIC	homozygous	115483471
12	17344392	17344393	A	G	31	GENIC	homozygous	115365080
12	17344595	17344596	C	T	25	GENIC	homozygous	115483472
12	17344670	17344671	T	C	23	GENIC	homozygous	115365081
12	17344807	17344808	T	C	20	GENIC	homozygous	115365082
12	17345026	17345027	T	C	25	GENIC	homozygous	115483473
12	17345142	17345143	T	C	34	GENIC	homozygous	115365083
12	17346189	17346190	A	G	29	GENIC	homozygous	115365085
12	17346271	17346272	T	C	25	GENIC	homozygous	115421341
12	17346364	17346365	T	C	24	GENIC	homozygous	115273561
12	17346988	17346989	C	T	37	GENIC	homozygous	115483474
12	17347062	17347063	A	G	43	GENIC	homozygous	115273563
12	17348064	17348065	T	G	13	GENIC	homozygous	115483475
12	17348738	17348739	A	G	17	GENIC	homozygous	115483476
12	17348831	17348832	A	G	22	GENIC	homozygous	115365086
12	17349307	17349308	T	C	26	GENIC	homozygous	115273565
12	17350727	17350728	G	A	24	GENIC	homozygous	115483477
12	17350951	17350952	G	A	32	GENIC	homozygous	115365087
12	17351964	17351965	T	C	25	GENIC	homozygous	115365088
12	17353329	17353330	A	G	41	GENIC	homozygous	115273573
12	17354336	17354337	A	T	23	GENIC	homozygous	115273575
12	17354338	17354339	T	G	22	GENIC	homozygous	115273576
12	17354515	17354516	A	G	15	GENIC	homozygous	115273580
12	17355178	17355179	G	A	15	GENIC	homozygous	115483478
12	17356326	17356327	C	T	26	GENIC	homozygous	115273584
12	17357452	17357453	G	C	24	GENIC	homozygous	115273586
12	17357535	17357536	T	C	26	GENIC	homozygous	115273588