chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
6	75671298	75671299	T	C	37	GENIC	homozygous	118554255
6	75671299	75671300	A	T	35	GENIC	homozygous	118554256
6	75671337	75671338	T	C	45	GENIC	homozygous	114861667
6	75684474	75684475	A	G	31	GENIC	homozygous	114861669
6	75685249	75685250	T	G	37	GENIC	homozygous	114861670
6	75685251	75685252	G	A	36	GENIC	homozygous	114861671
6	75685253	75685254	C	T	38	GENIC	homozygous	114861672
6	75686384	75686385	A	G	45	GENIC	homozygous	114861674
6	75686563	75686564	T	C	51	GENIC	homozygous	114861675
6	75687108	75687109	C	A	22	GENIC	homozygous	118554257
6	75687467	75687468	A	G	35	GENIC	homozygous	114861677
6	75687586	75687587	G	C	56	GENIC	homozygous	114861681
6	75687667	75687668	G	A	52	GENIC	homozygous	114861682
6	75687870	75687871	A	G	39	GENIC	homozygous	114861683
6	75687927	75687928	G	A	25	GENIC	homozygous	114861684
6	75687982	75687983	C	T	28	GENIC	homozygous	114861685
6	75688082	75688083	T	C	20	GENIC	homozygous	114861686
6	75688703	75688704	C	T	32	GENIC	homozygous	114861688
6	75689129	75689130	A	C	34	GENIC	homozygous	114861689
6	75690747	75690748	G	A	33	GENIC	possibly homozygous	114861690
6	75690755	75690756	G	A	21	GENIC	possibly homozygous	114861691
6	75690759	75690760	A	G	21	GENIC	possibly homozygous	118554258
6	75691072	75691073	T	C	40	GENIC	homozygous	114861692
6	75691758	75691759	T	C	22	GENIC	homozygous	114861693
6	75693549	75693550	A	C	41	GENIC	homozygous	114861695
6	75693983	75693984	T	C	29	GENIC	homozygous	114861696
6	75694892	75694893	T	C	43	GENIC	homozygous	114861699
6	75695195	75695196	C	T	36	GENIC	homozygous	114861700
6	75695521	75695522	T	C	39	GENIC	homozygous	114861710
6	75695649	75695650	T	C	44	GENIC	homozygous	114861711
6	75695672	75695673	T	C	49	GENIC	homozygous	114861712
6	75695990	75695991	A	G	61	GENIC	homozygous	114861713
6	75696257	75696258	G	T	9	GENIC	possibly homozygous	118554259
6	75696467	75696468	A	G	57	GENIC	homozygous	114861714
6	75697584	75697585	T	C	33	GENIC	homozygous	114861715
6	75697884	75697885	A	C	51	GENIC	homozygous	114861716
6	75697927	75697928	T	C	41	GENIC	homozygous	114861717