chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
1	81786146	81786147	A	G	7	GENIC	homozygous	60746823
1	81786188	81786189	T	G	10	GENIC	homozygous	60746824
1	81786191	81786192	C	G	9	GENIC	homozygous	60746825
1	81786210	81786211	C	G	10	GENIC	homozygous	60746826
1	81786211	81786212	C	T	10	GENIC	homozygous	60746827
1	81786216	81786217	T	G	10	GENIC	homozygous	60746828
1	81786234	81786235	C	-	7	GENIC	homozygous	60746829
1	81786251	81786252	C	G	8	GENIC	homozygous	61448617
1	81786534	81786535	T	C	7	GENIC	homozygous	60746832
1	81786535	81786536	G	A	8	GENIC	homozygous	60746833
1	81787320	81787321	G	GTCT	9	GENIC	heterozygous	60746834
1	81790102	81790103	A	AC	15	GENIC	heterozygous	60746835
1	81798068	81798069	C	CA	16	GENIC	homozygous	60746836
1	81806034	81806035	A	-	16	GENIC	heterozygous	60746837
1	81809853	81809854	C	-	4	GENIC	heterozygous	61448618
1	81810446	81810447	T	G	8	GENIC	homozygous	60746840
1	81810452	81810453	T	G	7	GENIC	homozygous	60746841
1	81810494	81810495	A	T	7	GENIC	homozygous	60746842
1	81810528	81810529	C	CTT	5	GENIC	homozygous	60746843