chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
12	32753972	32753973	T	C	46	GENIC	homozygous	115310070
12	32754911	32754912	C	T	44	GENIC	homozygous	115604423
12	32755507	32755508	T	C	17	GENIC	homozygous	115310072
12	32756667	32756668	C	A	24	GENIC	homozygous	115310074
12	32757445	32757446	A	T	21	GENIC	homozygous	115310080
12	32758080	32758081	A	G	17	GENIC	homozygous	115310082
12	32758915	32758916	C	T	34	GENIC	homozygous	115310084
12	32760805	32760806	C	T	50	GENIC	homozygous	115310086
12	32761899	32761900	T	C	51	GENIC	homozygous	115310090
12	32762668	32762669	T	G	33	GENIC	homozygous	115310092
12	32762692	32762693	G	A	32	GENIC	homozygous	115310094
12	32763267	32763268	C	T	44	GENIC	homozygous	115310098
12	32764602	32764603	A	G	31	GENIC	homozygous	115310102
12	32764706	32764707	A	G	35	GENIC	homozygous	115310104
12	32765019	32765020	A	G	45	GENIC	homozygous	115310106
12	32765034	32765035	T	C	46	GENIC	homozygous	115310108
12	32765136	32765137	G	C	65	GENIC	homozygous	115310110
12	32765298	32765299	T	C	30	GENIC	homozygous	115310112
12	32766855	32766856	C	T	48	GENIC	homozygous	115310114
12	32767318	32767319	T	C	41	GENIC	homozygous	115310116
12	32767658	32767659	A	G	20	GENIC	homozygous	115310118
12	32767733	32767734	T	C	41	GENIC	homozygous	115310120
12	32768497	32768498	C	G	31	GENIC	homozygous	115310122
12	32768864	32768865	A	G	43	GENIC	homozygous	115310124
12	32769268	32769269	A	G	46	GENIC	homozygous	115310126
12	32769277	32769278	C	T	39	GENIC	homozygous	115310128
12	32769447	32769448	T	A	47	GENIC	homozygous	115310130
12	32769830	32769831	T	C	26	GENIC	homozygous	115310132
12	32771105	32771106	T	C	47	GENIC	homozygous	115310136
12	32771543	32771544	T	C	32	GENIC	homozygous	115424460
12	32772089	32772090	A	G	39	GENIC	homozygous	115310140