chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
12	43423676	43423678	CC	--	4	GENIC	homozygous	50384063
12	43424330	43424331	C	T	10	GENIC	homozygous	50453093
12	43424728	43424729	T	C	17	GENIC	homozygous	50453094
12	43425577	43425579	AC	--	23	GENIC	homozygous	50384064
12	43425891	43425892	G	A	9	GENIC	homozygous	50384065
12	43427035	43427036	T	C	4	GENIC	heterozygous	50211731
12	43431246	43431247	A	ACTGTCTGT	8	GENIC	heterozygous	50610597
12	43432099	43432100	C	T	20	GENIC	homozygous	50453095
12	43433135	43433136	A	C	10	GENIC	homozygous	50211821
12	43433601	43433602	T	A	1	GENIC	homozygous	50211825
12	43435186	43435187	A	G	7	GENIC	homozygous	50384070
12	43436215	43436216	T	C	19	GENIC	homozygous	50211838
12	43439075	43439076	A	AG	22	GENIC	possibly homozygous	50211844
12	43440213	43440214	G	A	14	GENIC	homozygous	50211846
12	43440301	43440302	A	G	21	GENIC	possibly homozygous	50329865
12	43440555	43440556	T	C	26	GENIC	homozygous	50211848
12	43440887	43440888	C	T	17	GENIC	homozygous	50329868
12	43441003	43441004	A	G	14	GENIC	possibly homozygous	50329870
12	43441067	43441068	C	T	12	GENIC	homozygous	50329872
12	43441182	43441183	C	T	3	GENIC	homozygous	50329874
12	43441395	43441396	T	A	3	GENIC	homozygous	50211850
12	43441537	43441538	C	-	1	GENIC	homozygous	50329880
12	43442856	43442857	T	TCTA	4	GENIC	homozygous	50329882
12	43443568	43443569	G	GT	10	GENIC	possibly homozygous	50329884