chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
12	54187778	54187779	G	C	6	GENIC	homozygous	50260633
12	54188137	54188138	C	T	36	GENIC	homozygous	50260635
12	54188952	54188954	AA	--	1	GENIC	homozygous	50260641
12	54189473	54189474	C	A	10	GENIC	heterozygous	50260645
12	54190301	54190302	A	-	5	GENIC	homozygous	50260647
12	54190412	54190413	C	G	13	GENIC	homozygous	50260648
12	54190692	54190693	G	GA	8	GENIC	possibly homozygous	50260650
12	54191358	54191359	C	-	4	GENIC	heterozygous	50260654
12	54192676	54192677	T	C	27	GENIC	homozygous	50260662
12	54193388	54193389	G	A	17	GENIC	possibly homozygous	50260664
12	54193874	54193875	A	-	3	GENIC	homozygous	50260668
12	54194992	54195040	CTGCTTCAGGCTGCTGTGTACTAGCTGTCCTTGTGCCAGGCCCATCCC	------------------------------------------------	4	GENIC	heterozygous	50514493
12	54195623	54195624	C	T	19	GENIC	possibly homozygous	50260670
12	54195914	54195915	G	A	24	GENIC	possibly homozygous	50260672
12	54196213	54196214	G	GAATA	8	GENIC	homozygous	50260674