chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
3	166739132	166739133	T	C	78	GENIC	homozygous	57770390
3	166739436	166739437	G	A	52	GENIC	homozygous	57770391
3	166739575	166739576	C	A	61	GENIC	possibly homozygous	57770392
3	166739771	166739772	C	G	54	GENIC	homozygous	57770393
3	166740357	166740358	T	C	46	GENIC	homozygous	57770394
3	166740709	166740710	A	G	54	GENIC	homozygous	57770395
3	166741254	166741255	C	T	50	GENIC	homozygous	57770396
3	166741838	166741839	C	G	40	GENIC	homozygous	57770397
3	166741865	166741866	A	G	44	GENIC	possibly homozygous	57770398
3	166742009	166742010	A	G	53	GENIC	homozygous	57770399
3	166742344	166742345	A	AT	28	GENIC	heterozygous	57770400
3	166742366	166742367	T	TTGG	26	GENIC	heterozygous	57770401
3	166742406	166742407	G	A	32	GENIC	heterozygous	57770402
3	166742409	166742410	C	T	30	GENIC	heterozygous	57770403
3	166742412	166742413	C	G	31	GENIC	heterozygous	57770404
3	166742418	166742419	T	C	33	GENIC	heterozygous	57770405
3	166742474	166742475	A	AT	44	GENIC	possibly homozygous	57770406
3	166742474	166742475	A	ATT	44	GENIC	heterozygous	57770407
3	166742504	166742505	T	C	39	GENIC	homozygous	57770408
3	166742720	166742721	A	AT	11	GENIC	heterozygous	57770409
3	166742720	166742721	A	ATT	11	GENIC	heterozygous	57770410
3	166742740	166742743	TTT	---	22	GENIC	homozygous	57770411
3	166742933	166742934	T	C	56	GENIC	possibly homozygous	57770412
3	166743473	166743474	G	A	57	GENIC	possibly homozygous	57770413
3	166744739	166744740	C	CCTAT	13	GENIC	possibly homozygous	57770414
3	166745488	166745489	T	C	47	GENIC	homozygous	57770415