chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
6	105431891	105431892	C	T	36	GENIC	homozygous	137868313
6	105440331	105440332	A		12	GENIC	heterozygous	403824341
6	105440331	105440332	A	T	12	GENIC	heterozygous	403824342
6	105465769	105465770	T	C	42	GENIC	homozygous	137868327
6	105465940	105465941	A	G	39	GENIC	homozygous	137868328
6	105466771	105466783	ACACACACACAG		38	GENIC	homozygous	141786258
6	105466930	105466931	T	C	49	GENIC	homozygous	141856234
6	105467371	105467371		GT	36	GENIC	homozygous	144749777
6	105468053	105468054	G	C	54	GENIC	homozygous	137868329
6	105468892	105468893	C	T	48	GENIC	homozygous	141856235
6	105469009	105469010	C	T	43	GENIC	homozygous	141856236
6	105469054	105469054		T	37	GENIC	possibly homozygous	137701794
6	105469307	105469308	A	G	60	GENIC	homozygous	137868330
6	105470665	105470666	T	C	51	GENIC	homozygous	141856237
6	105470724	105470725	C	T	47	GENIC	homozygous	137868331
6	105470767	105470768	C	T	41	GENIC	homozygous	141856238
6	105471402	105471403	C	T	55	GENIC	homozygous	141856239
6	105471810	105471811	A	G	59	GENIC	homozygous	141856240
6	105472005	105472005		T	53	GENIC	homozygous	137701795
6	105472093	105472094	C	T	59	GENIC	homozygous	141856241