chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
1	97413139	97413140	T	C	12	GENIC	homozygous	141220762
1	97415783	97415784	A	G	9	GENIC	homozygous	141220763
1	97417139	97417140	C	T	15	GENIC	homozygous	141220764
1	97417587	97417588	A	G	18	GENIC	homozygous	141220765
1	97417588	97417589	T	A	18	GENIC	homozygous	141220766
1	97418677	97418678	T	A	17	GENIC	homozygous	141220767
1	97419069	97419069		C	14	GENIC	homozygous	141163669
1	97419120	97419120		C	14	GENIC	homozygous	141163670
1	97419148	97419149	T	C	16	GENIC	homozygous	141220768
1	97419194	97419195	T	A	17	GENIC	homozygous	141220769
1	97420197	97420197		A	14	GENIC	homozygous	141163671
1	97421891	97421892	C	T	13	GENIC	homozygous	141220770
1	97425055	97425056	C	T	30	GENIC	possibly homozygous	141220771
1	97426187	97426188	C	T	21	GENIC	homozygous	141220772
1	97429058	97429059	T	C	19	GENIC	homozygous	141220773
1	97429582	97429583	A	T	20	GENIC	homozygous	141220774
1	97429726	97429727	C	T	21	GENIC	homozygous	141220775
1	97429762	97429763	A	G	24	GENIC	homozygous	141220776
1	97432320	97432321	A	G	11	GENIC	homozygous	141220777
1	97436853	97436854	T	C	23	GENIC	homozygous	141220778
1	97437095	97437096	C	T	10	GENIC	homozygous	141220779
1	97439823	97439824	T	A	14	GENIC	homozygous	141220780
1	97441528	97441528		AGGAGGAGG	20	GENIC	homozygous	141163672
1	97425206	97425207	T		13	GENIC	heterozygous	402953299
1	97425206	97425207	T	C	13	GENIC	possibly homozygous	153868093
1	97437087	97437088	C		10	GENIC	homozygous	402953300
1	97437087	97437088	C	T	10	GENIC	heterozygous	402953301