chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
12	46862445	46862446	G	A	23	GENIC	homozygous	133011098
12	46863018	46863019	G	A	23	GENIC	homozygous	115486529
12	46863041	46863042	G	A	24	GENIC	homozygous	115486530
12	46863409	46863410	T	C	26	GENIC	homozygous	115397173
12	46863924	46863925	T	C	17	GENIC	homozygous	115486531
12	46864636	46864637	T	A	22	GENIC	homozygous	115342607
12	46864705	46864706	C	A	44	GENIC	homozygous	115342609
12	46865228	46865229	T	A	28	GENIC	homozygous	115397177
12	46867992	46867993	T	C	12	GENIC	homozygous	115486532
12	46869235	46869236	T	C	25	GENIC	homozygous	115342623
12	46869447	46869448	G	A	12	GENIC	homozygous	133011099
12	46869483	46869484	T	G	8	GENIC	homozygous	115486533
12	46870926	46870927	T	C	16	GENIC	homozygous	115342625
12	46871308	46871309	T	C	14	GENIC	homozygous	115342627
12	46871382	46871383	C	T	14	GENIC	homozygous	133011100
12	46871500	46871501	T	G	21	GENIC	homozygous	115342629
12	46873118	46873118		T	26	GENIC	homozygous	128996756
12	46868838	46868839	G		24	GENIC	homozygous	128996749
12	46869085	46869085		A	10	GENIC	possibly homozygous	128996750
12	46864917	46864917		TG	15	GENIC	homozygous	133010128
12	46865895	46865896	A	G	8	GENIC	homozygous	118272506
12	46873205	46873206	A	G	26	GENIC	homozygous	115342635
12	46874123	46874127	CTAT		12	GENIC	homozygous	133010129
12	46874224	46874224		C	30	GENIC	homozygous	133010130
12	46875285	46875286	A	G	16	GENIC	homozygous	115397193
12	46875435	46875436	A	G	14	GENIC	homozygous	115342637
12	46876107	46876108	C	T	20	GENIC	homozygous	115342639