chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
17	81939869	81939870	A	G	26	GENIC	homozygous	47204236
17	81940694	81940695	A	G	16	GENIC	homozygous	47204237
17	81941026	81941027	A	T	20	GENIC	homozygous	47204238
17	81941169	81941170	A	-	8	GENIC	homozygous	47204241
17	81941700	81941701	G	A	15	GENIC	homozygous	47456814
17	81941988	81941989	A	ATT	14	GENIC	possibly homozygous	47456816
17	81942391	81942392	C	T	14	GENIC	homozygous	47204244
17	81942607	81942608	G	A	14	GENIC	possibly homozygous	47204245
17	81942618	81942619	G	A	13	GENIC	homozygous	47204246
17	81942620	81942621	T	TA	13	GENIC	homozygous	47204247
17	81942690	81942691	T	-	9	GENIC	homozygous	47204248
17	81942773	81942774	A	G	20	GENIC	homozygous	47204249
17	81942778	81942779	C	T	18	GENIC	homozygous	47204250
17	81943134	81943135	T	C	13	GENIC	homozygous	47204251
17	81943162	81943163	A	AATATATAT	9	GENIC	homozygous	47601105
17	81943518	81943519	A	-	17	GENIC	homozygous	47456818
17	81943634	81943635	T	TG	13	GENIC	possibly homozygous	47204254
17	81944097	81944098	G	A	24	GENIC	homozygous	47204255
17	81944837	81944838	T	C	14	GENIC	homozygous	47204256
17	81944870	81944871	C	G	20	GENIC	homozygous	47204257