chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
12	40589857	40589858	C	T	12	GENIC	homozygous	139143344
12	40590106	40590107	A	T	17	GENIC	possibly homozygous	139143345
12	40590398	40590399	A	G	11	GENIC	homozygous	139143346
12	40591641	40591642	T	C	16	GENIC	homozygous	139143347
12	40592059	40592060	A	G	17	GENIC	homozygous	139143348
12	40592156	40592157	G	T	16	GENIC	homozygous	139143349
12	40595077	40595078	G	C	18	GENIC	homozygous	139143351
12	40595925	40595926	C	T	14	GENIC	homozygous	139143353
12	40596040	40596041	A	G	13	GENIC	heterozygous	404021352
12	40596040	40596041	A		13	GENIC	heterozygous	404021353
12	40596667	40596668	C	T	19	GENIC	homozygous	139143354
12	40598393	40598394	T	C	18	GENIC	homozygous	139143356