chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
3	60445999	60446000	A	G	23	GENIC	homozygous	119793341
3	60448682	60448683	T	C	31	GENIC	homozygous	111585438
3	60449211	60449212	A	G	15	GENIC	homozygous	111585440
3	60449584	60449585	G	A	24	GENIC	homozygous	119793343
3	60450478	60450479	G	A	25	GENIC	homozygous	111585443
3	60450517	60450518	A	G	27	GENIC	homozygous	111585444
3	60450945	60450946	G	A	32	GENIC	homozygous	119793345
3	60451045	60451046	C	T	26	GENIC	homozygous	111585445
3	60452043	60452044	G	C	1	GENIC	homozygous	119793347
3	60452927	60452928	G	T	23	GENIC	homozygous	111585448
3	60453482	60453483	C	T	26	GENIC	homozygous	111585449
3	60453972	60453973	T	C	35	GENIC	homozygous	111585450
3	60454072	60454073	C	A	32	GENIC	homozygous	111585451
3	60454774	60454775	G	A	31	GENIC	homozygous	111585454
3	60454830	60454831	G	A	38	GENIC	homozygous	111585455
3	60454865	60454866	C	G	38	GENIC	homozygous	111585456
3	60455227	60455228	A	C	37	GENIC	homozygous	111585457
3	60455394	60455395	C	T	26	GENIC	homozygous	119793349
3	60455830	60455831	T	C	33	GENIC	homozygous	111585458
3	60456252	60456253	C	A	24	GENIC	homozygous	111585459
3	60456457	60456458	A	G	24	GENIC	homozygous	111585461
3	60456502	60456503	T	C	28	GENIC	homozygous	111585462
3	60456630	60456631	A	G	29	GENIC	homozygous	111585463
3	60456697	60456698	G	C	29	GENIC	possibly homozygous	111585464
3	60456733	60456734	C	T	24	GENIC	homozygous	111585465
3	60456924	60456925	T	G	35	GENIC	homozygous	111585466
3	60456958	60456959	C	T	29	GENIC	homozygous	111585467
3	60457284	60457285	G	A	39	GENIC	homozygous	111585468
3	60457346	60457347	T	C	36	GENIC	homozygous	111585469
3	60457398	60457399	G	A	45	GENIC	homozygous	119793351
3	60458700	60458701	C	A	19	GENIC	homozygous	119793353
3	60459306	60459307	A	T	21	GENIC	homozygous	119793355
3	60460226	60460227	G	A	16	GENIC	homozygous	119793357
3	60460320	60460321	G	A	17	GENIC	homozygous	119793359
3	60460364	60460365	T	C	28	GENIC	homozygous	111585476
3	60460378	60460379	C	T	32	GENIC	homozygous	111585477