chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
12	42479561	42479562	A	T	17	GENIC	homozygous	50209153
12	42485831	42485832	A	G	8	GENIC	homozygous	50209163
12	42487729	42487730	T	C	14	GENIC	homozygous	50209169
12	42483132	42483133	G	A	9	GENIC	homozygous	51079214
12	42488256	42488257	A	G	16	GENIC	homozygous	50804595
12	42488606	42488607	C	T	15	GENIC	homozygous	50563866
12	42488909	42488910	A	T	17	GENIC	homozygous	50563868
12	42489036	42489037	C	T	20	GENIC	homozygous	50563870
12	42489914	42489915	C	T	15	GENIC	homozygous	50563872
12	42490252	42490253	G	-	19	GENIC	homozygous	50592216
12	42490538	42490539	A	G	13	GENIC	homozygous	50209176
12	42490657	42490658	C	T	17	GENIC	homozygous	50209180
12	42490876	42490877	A	C	17	GENIC	homozygous	50563880
12	42491236	42491237	A	-	22	GENIC	heterozygous	50327525
12	42491393	42491394	C	T	11	GENIC	homozygous	50209181
12	42493649	42493650	T	C	19	INTERGENIC	homozygous	50592219
12	42493679	42493680	G	A	19	INTERGENIC	homozygous	50804597
12	42493899	42493900	C	T	17	INTERGENIC	homozygous	50592220
12	42494101	42494102	C	A	20	INTERGENIC	homozygous	50209183
12	42494157	42494158	A	G	26	INTERGENIC	homozygous	50209184