chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
10	46110633	46110634	T	C	34	GENIC	homozygous	67948432
10	46111584	46111585	T	C	32	GENIC	homozygous	67948437
10	46111635	46111636	G	T	31	GENIC	homozygous	67948441
10	46112497	46112498	G	A	15	GENIC	heterozygous	67948445
10	46112525	46112526	G	T	16	GENIC	possibly homozygous	67948448
10	46112570	46112571	T	C	13	GENIC	homozygous	67948452
10	46112584	46112585	C	T	14	GENIC	homozygous	67948456
10	46112596	46112597	G	A	13	GENIC	homozygous	67948461
10	46112601	46112602	C	G	13	GENIC	homozygous	67948465
10	46113857	46113858	T	C	34	GENIC	homozygous	67948469
10	46114475	46114476	A	C	42	GENIC	homozygous	67948473
10	46115165	46115166	G	T	27	GENIC	homozygous	67948477
10	46115316	46115317	T	G	21	GENIC	homozygous	67948481
10	46115609	46115610	T	C	15	GENIC	possibly homozygous	67948494
10	46117492	46117493	T	C	44	GENIC	homozygous	67948498
10	46118390	46118391	G	A	41	GENIC	homozygous	67948502
10	46118438	46118439	A	G	48	GENIC	homozygous	67948506
10	46118842	46118843	T	C	38	GENIC	homozygous	67948510
10	46120408	46120409	C	T	46	GENIC	possibly homozygous	67948514
10	46120496	46120497	A	C	21	GENIC	homozygous	67948518
10	46122290	46122291	A	G	33	GENIC	heterozygous	68778187
10	46123215	46123216	G	A	31	GENIC	homozygous	67948522
10	46123317	46123318	G	A	46	GENIC	possibly homozygous	67948526
10	46124950	46124951	A	G	33	GENIC	possibly homozygous	67948530
10	46125792	46125793	G	A	32	GENIC	homozygous	67948534
10	46128759	46128760	A	G	23	GENIC	homozygous	67948538