chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
2	215913667	215913668	C	CTT	6	GENIC	heterozygous	60516812
2	215914565	215914566	C	G	17	GENIC	homozygous	60348582
2	215915882	215915883	A	G	31	GENIC	homozygous	60348584
2	215918059	215918060	T	C	12	GENIC	homozygous	60159679
2	215918753	215918754	A	ATCTG	20	GENIC	homozygous	60159680
2	215918791	215918792	C	CTTCT	15	GENIC	homozygous	60159681
2	215918852	215918853	C	CT	13	GENIC	possibly homozygous	60348586
2	215919732	215919733	G	GC	8	GENIC	homozygous	60348588
2	215919774	215919775	C	CT	8	GENIC	homozygous	60548704
2	215920059	215920060	T	C	16	GENIC	homozygous	60159686
2	215921410	215921411	G	A	22	GENIC	homozygous	60237655
2	215922524	215922525	G	A	18	GENIC	homozygous	60237656