chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
1	181173498	181173499	C	T	16	GENIC	homozygous	135762803
1	181173587	181173588	C	T	20	GENIC	homozygous	135762804
1	181173754	181173755	A		24	GENIC	homozygous	135448873
1	181173825	181173826	T	C	31	GENIC	homozygous	135762805
1	181173967	181173985	TGTGTACCACATGTGTTC		16	GENIC	homozygous	135448874
1	181174058	181174059	G	A	22	GENIC	homozygous	135762806
1	181174482	181174483	G	A	19	GENIC	homozygous	135762807
1	181174780	181174784	TGTC		20	GENIC	possibly homozygous	135448875
1	181175491	181175492	A	G	21	GENIC	homozygous	135762808
1	181176004	181176005	A	G	13	GENIC	homozygous	135762809
1	181176303	181176304	T	C	20	GENIC	homozygous	135762810
1	181176400	181176401	A	G	17	GENIC	homozygous	135762811
1	181177195	181177196	T	C	29	GENIC	homozygous	135762812
1	181177451	181177452	T	A	29	GENIC	possibly homozygous	135762813
1	181177662	181177663	G	A	24	GENIC	homozygous	135762814