chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
4	81207952	81207953	C	T	23	GENIC	homozygous	112748235
4	81208413	81208414	T	C	28	GENIC	homozygous	112748239
4	81208501	81208502	C	T	14	GENIC	homozygous	112748241
4	81213132	81213133	A	T	11	GENIC	homozygous	112748243
4	81213399	81213400	T	C	17	GENIC	homozygous	112748245
4	81213622	81213623	G	A	33	GENIC	homozygous	112748247
4	81216563	81216564	A	G	32	GENIC	homozygous	112748251
4	81218371	81218372	T	A	28	GENIC	homozygous	112748253
4	81219932	81219933	C	T	19	GENIC	homozygous	112748257
4	81220000	81220001	A	G	29	GENIC	homozygous	112748259
4	81220013	81220014	G	A	27	GENIC	homozygous	112748261
4	81221243	81221244	G	A	19	GENIC	homozygous	112748265
4	81221261	81221262	C	T	16	GENIC	homozygous	112748267
4	81222137	81222138	T	A	24	GENIC	homozygous	112748269
4	81223921	81223922	A	G	27	GENIC	homozygous	112748271
4	81225283	81225284	G	A	17	GENIC	homozygous	112748275
4	81225656	81225657	A	C	20	GENIC	homozygous	112748277
4	81226875	81226876	T	C	21	GENIC	homozygous	112748279
4	81227631	81227632	G	C	28	GENIC	homozygous	112748281
4	81230606	81230607	G	T	26	GENIC	homozygous	112748285