chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
12	42479561	42479562	A	T	2	GENIC	homozygous	50209153
12	42487729	42487730	T	C	20	GENIC	homozygous	50209169
12	42488256	42488257	A	G	6	GENIC	heterozygous	50804595
12	42488606	42488607	C	T	17	GENIC	homozygous	50563866
12	42488909	42488910	A	T	28	GENIC	homozygous	50563868
12	42489036	42489037	C	T	14	GENIC	possibly homozygous	50563870
12	42489914	42489915	C	T	29	GENIC	possibly homozygous	50563872
12	42490252	42490253	G	-	8	GENIC	homozygous	50592216
12	42490538	42490539	A	G	22	GENIC	homozygous	50209176
12	42490657	42490658	C	T	14	GENIC	homozygous	50209180
12	42490876	42490877	A	C	23	GENIC	possibly homozygous	50563880
12	42493649	42493650	T	C	2	INTERGENIC	heterozygous	50592219
12	42493679	42493680	G	A	6	INTERGENIC	heterozygous	50804597
12	42493899	42493900	C	T	25	INTERGENIC	homozygous	50592220
12	42494101	42494102	C	A	16	INTERGENIC	possibly homozygous	50209183
12	42494157	42494158	A	G	21	INTERGENIC	possibly homozygous	50209184