chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
12	40772381	40772382	G	-	18	GENIC	homozygous	50949235
12	40772428	40772429	G	-	16	GENIC	homozygous	50204648
12	40773342	40773343	G	-	21	GENIC	homozygous	50204650
12	40773346	40773347	G	A	21	GENIC	homozygous	50512471
12	40773818	40773819	T	C	38	GENIC	homozygous	50204651
12	40774068	40774069	G	GA	10	GENIC	homozygous	50592140
12	40774237	40774238	A	C	16	GENIC	possibly homozygous	50323422
12	40774751	40774752	C	T	24	GENIC	homozygous	50640208
12	40775477	40775478	G	C	20	GENIC	homozygous	50949238
12	40775852	40775853	G	T	37	GENIC	homozygous	50204652
12	40776471	40776472	T	C	21	GENIC	homozygous	50949241