chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
12	39428717	39428718	G	GTCA	37	GENIC	heterozygous	50543022
12	39428758	39428759	T	TG	31	GENIC	heterozygous	50543023
12	39428832	39428833	G	GGGATCCTA	20	GENIC	heterozygous	50543024
12	39428923	39428933	GTGTGGGCTT	----------	20	GENIC	heterozygous	50543025
12	39428935	39428941	TAATTT	------	19	GENIC	heterozygous	50543026
12	39428941	39428942	C	CG	18	GENIC	heterozygous	50543027
12	39429159	39429160	G	GT	8	GENIC	homozygous	50199241
12	39429854	39429870	GTGTGTGTGTGTGTGT	----------------	9	GENIC	heterozygous	50907928
12	39432504	39432505	G	A	14	GENIC	heterozygous	50199255
12	39432536	39432549	AGAAAAAAAAAAG	-------------	4	GENIC	heterozygous	50543030
12	39433578	39433588	ACACACACAC	----------	17	GENIC	homozygous	50946479
12	39434217	39434218	C	A	43	GENIC	homozygous	50199263
12	39434266	39434267	G	GT	34	GENIC	homozygous	50199265
12	39435325	39435326	T	C	31	GENIC	homozygous	50946484
12	39435622	39435623	T	C	28	GENIC	homozygous	50946487
12	39436026	39436031	GAACC	-----	4	GENIC	heterozygous	50199271
12	39436684	39436685	A	G	30	GENIC	homozygous	50946490
12	39438398	39438399	T	C	26	GENIC	possibly homozygous	50199279
12	39440482	39440483	C	G	18	GENIC	homozygous	50199292
12	39441992	39441993	G	GT	26	GENIC	homozygous	50199300
12	39442254	39442255	T	TA	12	GENIC	heterozygous	50199302
12	39445390	39445391	A	G	23	GENIC	homozygous	50199314
12	39445397	39445398	T	TG	22	GENIC	homozygous	50511705
12	39447466	39447469	AAA	---	17	GENIC	heterozygous	50412826
12	39447467	39447469	AA	--	17	GENIC	possibly homozygous	50543034
12	39447593	39447594	A	C	26	GENIC	homozygous	50946493
12	39447907	39447919	TATTTATTTATT	------------	1	GENIC	homozygous	50946496
12	39450732	39450733	G	GAAAAAA	4	GENIC	homozygous	50543036
12	39450939	39450940	G	GA	10	GENIC	heterozygous	50199338
12	39450939	39450940	G	GAA	10	GENIC	possibly homozygous	50558896