chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
10	46110633	46110634	T	C	19	GENIC	homozygous	67948432
10	46111584	46111585	T	C	34	GENIC	homozygous	67948437
10	46111635	46111636	G	T	31	GENIC	homozygous	67948441
10	46112426	46112427	A	T	19	GENIC	possibly homozygous	69187367
10	46113857	46113858	T	C	21	GENIC	homozygous	67948469
10	46114475	46114476	A	C	26	GENIC	homozygous	67948473
10	46115165	46115166	G	T	40	GENIC	homozygous	67948477
10	46115316	46115317	T	G	23	GENIC	homozygous	67948481
10	46117492	46117493	T	C	24	GENIC	homozygous	67948498
10	46118390	46118391	G	A	23	GENIC	homozygous	67948502
10	46118438	46118439	A	G	27	GENIC	homozygous	67948506
10	46118842	46118843	T	C	17	GENIC	homozygous	67948510
10	46120408	46120409	C	T	18	GENIC	homozygous	67948514
10	46120496	46120497	A	C	19	GENIC	possibly homozygous	67948518
10	46123215	46123216	G	A	29	GENIC	homozygous	67948522
10	46123317	46123318	G	A	29	GENIC	homozygous	67948526
10	46124950	46124951	A	G	22	GENIC	homozygous	67948530
10	46125792	46125793	G	A	23	GENIC	homozygous	67948534
10	46128759	46128760	A	G	19	GENIC	homozygous	67948538