chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
8	76655241	76655242	T	C	8	GENIC	possibly homozygous	53128070
8	76655314	76655315	G	A	6	GENIC	homozygous	53128071
8	76657154	76657155	A	G	15	GENIC	possibly homozygous	53128072
8	76658014	76658015	G	A	11	GENIC	homozygous	53128073
8	76659570	76659571	T	-	2	GENIC	heterozygous	53128075
8	76660033	76660034	A	G	15	GENIC	homozygous	53128076
8	76660949	76660950	T	C	14	GENIC	homozygous	53128077
8	76663408	76663409	T	C	12	GENIC	heterozygous	53128079
8	76664085	76664086	G	C	15	GENIC	homozygous	53128081
8	76666330	76666331	C	T	15	GENIC	possibly homozygous	53128082
8	76666465	76666466	C	CA	4	GENIC	heterozygous	53128083
8	76666842	76666843	A	G	14	GENIC	homozygous	53128084
8	76667131	76667132	T	C	13	GENIC	homozygous	53128085
8	76667146	76667147	C	T	10	GENIC	homozygous	53128086
8	76669439	76669441	AG	--	3	GENIC	heterozygous	53396769
8	76671812	76671813	T	G	11	GENIC	homozygous	53128088
8	76672417	76672418	G	A	13	GENIC	homozygous	53128089
8	76672486	76672487	T	C	12	GENIC	homozygous	53128090
8	76673893	76673894	C	T	17	GENIC	possibly homozygous	53630076
8	76674134	76674135	C	T	15	GENIC	homozygous	53128091
8	76674817	76674818	C	CCCA	1	GENIC	homozygous	53128092
8	76675388	76675389	T	C	4	GENIC	homozygous	53128094