chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
3	72461578	72461579	G	A	29	GENIC	homozygous	111608085
3	72461858	72461859	C	T	27	GENIC	homozygous	111608086
3	72462875	72462876	G	T	37	GENIC	homozygous	111608088
3	72463146	72463147	A	G	31	GENIC	possibly homozygous	119675448
3	72463428	72463429	T	A	31	GENIC	homozygous	119868456
3	72464241	72464242	T	G	29	GENIC	homozygous	111608093
3	72464453	72464454	A	C	24	GENIC	homozygous	111608094
3	72466478	72466479	A	G	34	GENIC	homozygous	111608103
3	72466669	72466670	A	G	33	GENIC	homozygous	111608105
3	72467137	72467138	G	A	35	GENIC	possibly homozygous	119675449
3	72467144	72467145	T	G	34	GENIC	possibly homozygous	111608107
3	72467793	72467794	A	G	34	GENIC	homozygous	119675450
3	72467847	72467848	T	A	34	GENIC	homozygous	111608108
3	72468885	72468886	C	A	25	GENIC	homozygous	119675451
3	72469383	72469384	T	C	30	GENIC	homozygous	111608112
3	72470213	72470214	A	C	21	GENIC	homozygous	119675452
3	72471221	72471222	C	A	14	GENIC	homozygous	111608115
3	72471235	72471236	G	A	12	GENIC	homozygous	119675453
3	72471501	72471502	G	A	12	GENIC	homozygous	119868458
3	72471562	72471563	C	T	19	GENIC	homozygous	119675454
3	72471980	72471981	T	A	20	GENIC	homozygous	111608117
3	72472022	72472023	C	T	13	GENIC	homozygous	119675455
3	72473623	72473624	T	C	28	GENIC	homozygous	119868460
3	72473663	72473664	G	T	19	GENIC	homozygous	119868462
3	72475921	72475922	C	T	27	GENIC	homozygous	111608126
3	72476990	72476991	C	T	29	GENIC	homozygous	111608128
3	72478832	72478833	C	T	30	GENIC	homozygous	111608129
3	72479618	72479619	T	C	35	GENIC	homozygous	111608130
3	72479646	72479647	C	G	34	GENIC	homozygous	111608131
3	72479660	72479661	G	A	38	GENIC	homozygous	111608132
3	72481032	72481033	A	G	22	GENIC	homozygous	111608134
3	72481807	72481808	A	C	33	GENIC	homozygous	111608135
3	72480131	72480132	G	C	24	GENIC	homozygous	119893796