chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
10	46110633	46110634	T	C	26	GENIC	possibly homozygous	67948432
10	46111584	46111585	T	C	14	GENIC	homozygous	67948437
10	46111635	46111636	G	T	8	GENIC	homozygous	67948441
10	46113857	46113858	T	C	9	GENIC	homozygous	67948469
10	46114475	46114476	A	C	17	GENIC	homozygous	67948473
10	46115165	46115166	G	T	9	GENIC	possibly homozygous	67948477
10	46115316	46115317	T	G	9	GENIC	homozygous	67948481
10	46115742	46115743	C	T	7	GENIC	possibly homozygous	82729781
10	46115763	46115764	C	T	6	GENIC	heterozygous	82711105
10	46117492	46117493	T	C	19	GENIC	homozygous	67948498
10	46118390	46118391	G	A	17	GENIC	homozygous	67948502
10	46118438	46118439	A	G	15	GENIC	homozygous	67948506
10	46118842	46118843	T	C	20	GENIC	homozygous	67948510
10	46120408	46120409	C	T	12	GENIC	homozygous	67948514
10	46120496	46120497	A	C	8	GENIC	homozygous	67948518
10	46123215	46123216	G	A	6	GENIC	homozygous	67948522
10	46123317	46123318	G	A	7	GENIC	homozygous	67948526
10	46124950	46124951	A	G	11	GENIC	homozygous	67948530
10	46125792	46125793	G	A	19	GENIC	homozygous	67948534
10	46128759	46128760	A	G	23	GENIC	homozygous	67948538
10	46112426	46112427	A	T	7	GENIC	homozygous	69187367