chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
12	42479561	42479562	A	T	5	GENIC	homozygous	50209153
12	42479566	42479567	T	G	5	GENIC	homozygous	50209154
12	42479572	42479573	T	C	5	GENIC	homozygous	50209155
12	42480660	42480661	C	CCA	5	GENIC	heterozygous	50209156
12	42480660	42480661	C	CCACA	5	GENIC	heterozygous	50544348
12	42483114	42483157	AGATGGGTGCTCTTAACCGCTGAGCCATCTCTCCAGCCCCCCC	-------------------------------------------	10	GENIC	heterozygous	50544349
12	42485028	42485029	G	GT	3	GENIC	homozygous	50572257
12	42485029	42485030	G	GT	4	GENIC	homozygous	50572259
12	42487706	42487707	C	T	7	GENIC	homozygous	50209168
12	42488113	42488114	A	ATTTTT	6	GENIC	heterozygous	50544352
12	42488411	42488421	TTTTTTTTAA	----------	7	GENIC	homozygous	50209172
12	42488455	42488456	C	-	5	GENIC	homozygous	50327515
12	42487194	42487195	G	A	8	GENIC	homozygous	50327513
12	42490593	42490594	A	G	7	GENIC	homozygous	50327517
12	42490595	42490596	A	-	7	GENIC	homozygous	50327519
12	42490603	42490609	CACACA	------	9	GENIC	possibly homozygous	50327521
12	42490657	42490658	C	T	11	GENIC	homozygous	50209180
12	42491236	42491237	A	-	7	GENIC	homozygous	50327525
12	42492918	42492919	C	T	9	GENIC	homozygous	50327527
12	42494101	42494102	C	A	13	INTERGENIC	homozygous	50209183