chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
10	97650014	97650015	G	A	8	GENIC	homozygous	126390564
10	97651075	97651076	G	A	22	GENIC	homozygous	126390565
10	97654286	97654287	A	T	17	GENIC	homozygous	126390566
10	97657785	97657786	A	G	29	GENIC	homozygous	126390567
10	97658656	97658657	C	T	14	GENIC	homozygous	126390568
10	97659675	97659676	A	G	15	GENIC	homozygous	126390569
10	97661996	97661997	C	T	21	GENIC	homozygous	126390570
10	97665137	97665138	A	C	20	GENIC	homozygous	126390571
10	97665734	97665735	T	C	16	GENIC	homozygous	126390572
10	97666541	97666542	T	C	10	GENIC	homozygous	126390573
10	97668177	97668178	G	A	21	GENIC	homozygous	126390574
10	97668881	97668882	T	C	11	GENIC	homozygous	126390575
10	97668899	97668900	T	C	7	GENIC	homozygous	126390576
10	97669096	97669097	C	T	12	GENIC	homozygous	126390577
10	97669928	97669929	A	G	22	GENIC	homozygous	126390578
10	97671218	97671219	T	C	10	GENIC	homozygous	126390579
10	97672978	97672979	C	T	10	GENIC	homozygous	126390580
10	97673872	97673873	C	T	21	GENIC	homozygous	126390581
10	97674477	97674478	A	T	21	GENIC	homozygous	126390582
10	97674975	97674976	G	A	19	GENIC	homozygous	126390583
10	97675290	97675291	T	C	17	GENIC	homozygous	126390584
10	97676110	97676111	T	C	24	GENIC	homozygous	126390585
10	97677005	97677006	G	T	20	GENIC	homozygous	126390586
10	97677148	97677149	T	C	19	GENIC	possibly homozygous	126390587
10	97677458	97677459	G	A	19	GENIC	homozygous	126390588
10	97678187	97678188	G	A	15	GENIC	homozygous	126390589
10	97678196	97678197	A	C	17	GENIC	homozygous	126390590
10	97678400	97678401	T	G	13	GENIC	homozygous	126390591
10	97678444	97678445	A	T	11	GENIC	homozygous	126390592
10	97678448	97678449	C	T	13	GENIC	homozygous	126390593