chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
6	105410409	105410413	AAAG		27	GENIC	homozygous	146149076
6	105417067	105417067		CTTC	12	GENIC	possibly homozygous	146432905
6	105431891	105431892	C	T	25	GENIC	homozygous	137868313
6	105465769	105465770	T	C	22	GENIC	homozygous	137868327
6	105465940	105465941	A	G	24	GENIC	homozygous	137868328
6	105468053	105468054	G	C	21	GENIC	homozygous	137868329
6	105469054	105469054		T	17	GENIC	possibly homozygous	137701794
6	105469307	105469308	A	G	29	GENIC	homozygous	137868330
6	105470724	105470725	C	T	33	GENIC	homozygous	137868331
6	105471402	105471403	C	T	28	GENIC	homozygous	141856239
6	105463261	105463262	G		22	GENIC	heterozygous	403894380
6	105463261	105463262	G	A	22	GENIC	heterozygous	403894381
6	105466771	105466783	ACACACACACAG		26	GENIC	homozygous	141786258
6	105466930	105466931	T	C	24	GENIC	homozygous	141856234
6	105468892	105468893	C	T	30	GENIC	homozygous	141856235
6	105469009	105469010	C	T	22	GENIC	homozygous	141856236
6	105470665	105470666	T	C	27	GENIC	homozygous	141856237
6	105470767	105470768	C	T	34	GENIC	homozygous	141856238
6	105467371	105467371		GT	11	GENIC	homozygous	144749777
6	105471810	105471811	A	G	16	GENIC	homozygous	141856240
6	105472005	105472005		T	21	GENIC	homozygous	137701795
6	105472093	105472094	C	T	18	GENIC	homozygous	141856241