chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
12	40911118	40911119	G	A	13	GENIC	homozygous	50452495
12	40912374	40912375	A	-	4	GENIC	homozygous	50422981
12	40912420	40912421	C	A	13	GENIC	possibly homozygous	50452496
12	40914020	40914021	C	-	17	GENIC	possibly homozygous	50452497
12	40914306	40914307	T	C	14	GENIC	homozygous	50205006
12	40914420	40914421	T	A	16	GENIC	homozygous	50452498
12	40916056	40916057	G	A	14	GENIC	possibly homozygous	50512488
12	40916202	40916204	TC	--	1	GENIC	homozygous	50452499
12	40916623	40916626	ATA	---	10	GENIC	possibly homozygous	50452500
12	40917344	40917345	A	G	11	GENIC	homozygous	50205012
12	40917780	40917781	T	C	5	GENIC	homozygous	50205014