chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
12	24251737	24251738	T	A	19	GENIC	homozygous	50132578
12	24251970	24251971	G	A	13	GENIC	homozygous	50132580
12	24252546	24252547	C	T	12	GENIC	homozygous	50132582
12	24253644	24253647	TGC	---	4	GENIC	homozygous	50132584
12	24253850	24253851	C	T	13	GENIC	homozygous	50132586
12	24255760	24255761	A	AGCT	15	GENIC	possibly homozygous	50132588
12	24256335	24256336	A	T	20	GENIC	homozygous	50132590
12	24258655	24258656	T	C	19	GENIC	homozygous	50132592
12	24259304	24259307	AAC	---	18	GENIC	homozygous	50132594
12	24259588	24259589	C	T	29	GENIC	homozygous	50132596