chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
12	42487729	42487730	T	C	17	GENIC	homozygous	50209169
12	42488256	42488257	A	G	16	GENIC	homozygous	50804595
12	42488606	42488607	C	T	23	GENIC	homozygous	50563866
12	42488909	42488910	A	T	19	GENIC	homozygous	50563868
12	42489036	42489037	C	T	23	GENIC	homozygous	50563870
12	42489914	42489915	C	T	34	GENIC	possibly homozygous	50563872
12	42490538	42490539	A	G	27	GENIC	homozygous	50209176
12	42490598	42490603	CACGC	-----	12	GENIC	heterozygous	50885553
12	42490657	42490658	C	T	23	GENIC	homozygous	50209180
12	42490876	42490877	A	C	24	GENIC	homozygous	50563880
12	42491393	42491394	C	T	7	GENIC	homozygous	50209181
12	42490252	42490253	G	-	40	GENIC	homozygous	50592216