chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
2	215913667	215913668	C	CT	11	GENIC	heterozygous	59391567
2	215913668	215913672	TTTT	----	11	GENIC	possibly homozygous	60082652
2	215913694	215913695	C	T	25	GENIC	heterozygous	59391568
2	215915065	215915066	C	G	21	GENIC	heterozygous	60159674
2	215917647	215917649	CT	--	12	GENIC	possibly homozygous	60159678
2	215918059	215918060	T	C	14	GENIC	homozygous	60159679
2	215918753	215918754	A	ATCTG	12	GENIC	homozygous	60159680
2	215919648	215919649	C	G	10	GENIC	homozygous	60159683
2	215920059	215920060	T	C	36	GENIC	homozygous	60159686
2	215921410	215921411	G	A	30	GENIC	homozygous	60237655
2	215915687	215915688	C	T	34	GENIC	homozygous	60237649
2	215919860	215919861	A	T	27	GENIC	homozygous	60237651
2	215920578	215920579	G	T	29	GENIC	homozygous	60237653
2	215922524	215922525	G	A	45	GENIC	homozygous	60237656