chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
10	4134927	4134929	TA	--	31	GENIC	heterozygous	51305719
10	4134935	4134937	TA	--	25	GENIC	heterozygous	51305720
10	4134935	4134936	T	TTG	25	GENIC	heterozygous	51305721
10	4134936	4134937	A	AGG	25	GENIC	heterozygous	51305722
10	4134939	4134940	T	G	37	GENIC	heterozygous	51608651
10	4134942	4134945	GTC	---	25	GENIC	heterozygous	51608652
10	4137746	4137747	C	A	24	GENIC	possibly homozygous	51305732
10	4137762	4137763	G	C	19	GENIC	homozygous	51305733
10	4137778	4137779	T	G	17	GENIC	homozygous	51305734
10	4137784	4137785	T	G	16	GENIC	homozygous	51305735
10	4137785	4137786	T	A	16	GENIC	homozygous	51305736
10	4137793	4137794	G	C	15	GENIC	homozygous	51305737
10	4137795	4137796	G	C	15	GENIC	homozygous	51305738
10	4137802	4137803	G	A	14	GENIC	homozygous	51305741
10	4137824	4137825	G	A	20	GENIC	homozygous	51305742
10	4137831	4137832	T	C	25	GENIC	homozygous	51305743
10	4137842	4137843	T	C	23	GENIC	homozygous	51305744
10	4137846	4137847	T	C	26	GENIC	homozygous	51305745
10	4137860	4137861	T	A	37	GENIC	homozygous	51305746
10	4137913	4137914	T	-	60	GENIC	homozygous	51305749
10	4138116	4138119	CGT	---	74	GENIC	homozygous	51305752
10	4142397	4142398	C	CCA	27	GENIC	heterozygous	51305781
10	4142410	4142411	T	-	33	GENIC	heterozygous	51305782
10	4143758	4143759	A	G	26	GENIC	heterozygous	51305794
10	4148571	4148572	C	T	47	GENIC	heterozygous	51305817
10	4148673	4148674	A	G	69	GENIC	heterozygous	52022283
10	4148684	4148685	G	A	66	GENIC	heterozygous	51305822
10	4148690	4148691	T	C	62	GENIC	heterozygous	51305823
10	4148836	4148837	C	T	38	GENIC	heterozygous	51608695
10	4148845	4148846	T	C	39	GENIC	heterozygous	51305827
10	4148872	4148873	A	G	32	GENIC	heterozygous	51608697
10	4148998	4148999	T	C	65	GENIC	heterozygous	51305828