chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
13	101476216	101476217	C	A	7	GENIC	homozygous	66168221
13	101476217	101476218	C	G	7	GENIC	homozygous	66168224
13	101476218	101476219	C	G	7	GENIC	homozygous	66168227
13	101476219	101476220	C	G	7	GENIC	homozygous	66168230
13	101476220	101476221	C	T	8	GENIC	homozygous	66168233
13	101477128	101477129	C	T	17	GENIC	homozygous	66380630
13	101488049	101488050	C	T	65	GENIC	heterozygous	66168245
13	101488088	101488089	C	T	29	GENIC	possibly homozygous	66168248
13	101488097	101488098	C	T	22	GENIC	homozygous	66168251
13	101488151	101488152	C	T	6	GENIC	homozygous	66168253
13	101488172	101488173	A	T	12	GENIC	homozygous	66168256
13	101488184	101488185	C	T	14	GENIC	possibly homozygous	66168259
13	101488973	101488974	A	G	9	GENIC	homozygous	66380696
13	101489615	101489616	T	G	10	GENIC	homozygous	66380704
13	101487866	101487867	C	T	28	GENIC	heterozygous	83261637
13	101487675	101487676	T	C	15	GENIC	heterozygous	83261635
13	101487806	101487807	C	T	19	GENIC	homozygous	83261636