chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
12	50285589	50285590	T	C	39	GENIC	heterozygous	115403399
12	50286895	50286896	C	G	14	GENIC	possibly homozygous	115351952
12	50287755	50287756	T	A	22	GENIC	homozygous	115351954
12	50288367	50288368	T	G	14	GENIC	homozygous	115351956
12	50288443	50288444	C	A	25	GENIC	homozygous	115351958
12	50289086	50289087	T	G	26	GENIC	homozygous	115351960
12	50291593	50291594	T	A	24	GENIC	homozygous	115351962
12	50297003	50297004	T	C	10	GENIC	homozygous	115452233
12	50300607	50300608	A	T	20	GENIC	homozygous	115351964
12	50306573	50306574	G	A	28	GENIC	homozygous	115351966
12	50310633	50310634	T	C	7	GENIC	heterozygous	115351968
12	50292669	50292670	G	A	30	GENIC	homozygous	115444425
12	50310696	50310697	G	A	11	GENIC	heterozygous	118274577
12	50310705	50310706	A	G	14	GENIC	possibly homozygous	118274578
12	50310762	50310763	T	C	46	GENIC	heterozygous	118274579
12	50310768	50310769	T	C	48	GENIC	heterozygous	118274580
12	50310778	50310779	A	G	54	GENIC	heterozygous	118274581
12	50310795	50310796	C	T	55	GENIC	heterozygous	118274584
12	50310822	50310823	T	C	43	GENIC	heterozygous	118328044
12	50311404	50311405	T	C	20	GENIC	homozygous	115351970
12	50311497	50311498	T	C	15	GENIC	homozygous	115351972