chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
12	26651270	26651271	G	C	11	GENIC	homozygous	50149388
12	26651302	26651303	G	C	14	GENIC	homozygous	50149390
12	26651357	26651358	G	A	14	GENIC	homozygous	50149392
12	26651405	26651406	G	-	10	GENIC	homozygous	50149394
12	26651524	26651525	C	T	21	GENIC	homozygous	50439742
12	26653692	26653693	G	GA	37	GENIC	homozygous	50439744
12	26653904	26653905	C	CACAT	17	GENIC	homozygous	50149396
12	26653915	26653916	A	G	35	GENIC	heterozygous	50439746
12	26653923	26653924	A	G	36	GENIC	heterozygous	50149398
12	26654406	26654407	C	T	41	GENIC	possibly homozygous	50439748