chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
17	80961842	80961843	T	C	14	GENIC	homozygous	111217806
17	80961857	80961858	G	C	16	GENIC	homozygous	111217807
17	80962125	80962126	C	T	21	GENIC	homozygous	111217808
17	80962279	80962280	C	A	20	GENIC	homozygous	111217809
17	80962891	80962892	G	C	5	GENIC	heterozygous	125634969
17	80963879	80963880	G	A	25	GENIC	homozygous	111217810
17	80963901	80963902	T	A	23	GENIC	homozygous	111217811
17	80964521	80964522	T	C	13	GENIC	homozygous	111217812
17	80965745	80965746	G	A	12	GENIC	homozygous	111217813
17	80966452	80966453	C	A	8	GENIC	homozygous	111217814
17	80966514	80966515	T	G	6	GENIC	homozygous	111217815
17	80966865	80966866	A	G	16	GENIC	homozygous	111217816
17	80967074	80967075	T	C	7	GENIC	homozygous	111217817
17	80967081	80967082	C	T	8	GENIC	homozygous	111217818
17	80967118	80967119	T	C	5	GENIC	homozygous	111217819
17	80967140	80967141	C	T	10	GENIC	homozygous	111217820
17	80967226	80967227	C	T	18	GENIC	homozygous	111217821
17	80967297	80967298	A	C	19	GENIC	homozygous	111217822
17	80967330	80967331	G	A	19	GENIC	homozygous	111217823
17	80967433	80967434	T	C	17	GENIC	homozygous	111217824
17	80967532	80967533	C	G	12	GENIC	homozygous	111217825
17	80967534	80967535	G	A	12	GENIC	homozygous	111217826
17	80965653	80965654	G	A	23	GENIC	homozygous	111283186
17	80970365	80970366	A	G	8	GENIC	homozygous	111112908
17	81000553	81000554	C	T	24	GENIC	homozygous	111112998