chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
2	57874514	57874515	G	A	55	GENIC	heterozygous	132280358
2	57878984	57878984		C	8	GENIC	homozygous	127626067
2	57894642	57894643	A		29	GENIC	homozygous	127626070
2	57894654	57894656	AC		28	GENIC	homozygous	127626071
2	57894683	57894683		C	20	GENIC	homozygous	127626072
2	57894724	57894724		T	46	GENIC	homozygous	127626073
2	57894748	57894748		AG	36	GENIC	homozygous	127626074
2	57894757	57894757		G	35	GENIC	homozygous	127626075
2	57894764	57894765	C		35	GENIC	homozygous	127626076
2	57894779	57894779		G	32	GENIC	homozygous	127626077
2	57894782	57894783	A	G	32	GENIC	homozygous	121382974
2	57894835	57894836	C		14	GENIC	homozygous	127626082
2	57894512	57894513	C	T	40	GENIC	possibly homozygous	120168340
2	57894790	57894790		G	28	GENIC	homozygous	127626078
2	57894806	57894807	G		22	GENIC	homozygous	127626079
2	57894823	57894823		GGGAG	16	GENIC	homozygous	127626080
2	57894830	57894832	AC		14	GENIC	homozygous	127626081
2	57894848	57894851	CGC		10	GENIC	homozygous	127626083
2	57894853	57894854	A	G	8	GENIC	homozygous	121382981
2	57894857	57894857		G	7	GENIC	homozygous	127626084
2	57894872	57894873	A		5	GENIC	homozygous	127626085
2	57894891	57894891		T	5	GENIC	homozygous	127626086
2	57894933	57894933		G	7	GENIC	homozygous	127626087
2	57894934	57894935	G	T	8	GENIC	homozygous	121382985
2	57894939	57894940	A	T	9	GENIC	homozygous	110534095
2	57894947	57894948	A		10	GENIC	homozygous	127626088
2	57901984	57901985	G		42	GENIC	homozygous	127626091
2	57901997	57901998	C		45	GENIC	homozygous	127626092
2	57902001	57902002	C	T	46	GENIC	homozygous	110534097
2	57902002	57902003	C	A	46	GENIC	homozygous	109770687
2	57902005	57902006	C	G	47	GENIC	homozygous	109770689
2	57902013	57902014	C	A	46	GENIC	homozygous	109770691