chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
12	28337072	28337073	A	G	27	GENIC	possibly homozygous	50420466
12	28337135	28337137	TA	--	13	GENIC	homozygous	50420467
12	28337152	28337153	C	A	18	GENIC	homozygous	50158534
12	28337391	28337392	A	AGG	1	GENIC	homozygous	50509762
12	28337401	28337404	TTC	---	1	GENIC	homozygous	50509764
12	28337421	28337422	T	C	5	GENIC	heterozygous	50420468
12	28337523	28337524	A	G	8	GENIC	homozygous	50420469
12	28337530	28337531	G	A	12	GENIC	homozygous	50420470
12	28337735	28337736	A	G	8	GENIC	homozygous	50420471
12	28337858	28337859	C	T	12	GENIC	homozygous	50158540
12	28337878	28337879	T	C	19	GENIC	homozygous	50420473
12	28338169	28338170	T	A	18	GENIC	possibly homozygous	50420482
12	28338181	28338182	C	T	16	GENIC	homozygous	50420483
12	28338313	28338314	C	T	6	GENIC	homozygous	50420484
12	28338325	28338326	G	A	6	GENIC	homozygous	50420485
12	28338364	28338365	A	G	19	GENIC	possibly homozygous	50420486
12	28338712	28338713	A	T	13	GENIC	heterozygous	50420487
12	28338714	28338715	T	-	15	GENIC	heterozygous	50304966
12	28338937	28338938	C	T	13	GENIC	homozygous	50158548
12	28340629	28340630	G	A	10	GENIC	homozygous	50158562
12	28340681	28340682	G	GT	1	GENIC	homozygous	50158564
12	28340933	28340934	T	TG	2	GENIC	heterozygous	50304970
12	28342904	28342905	C	A	22	GENIC	possibly homozygous	50158594
12	28342987	28342989	GA	--	1	GENIC	homozygous	50509766
12	28345264	28345265	C	CT	12	GENIC	heterozygous	50420489
12	28345348	28345349	A	T	5	GENIC	homozygous	50420490
12	28345850	28345851	C	T	14	GENIC	homozygous	50420491
12	28348283	28348284	C	A	8	GENIC	possibly homozygous	50158626
12	28348413	28348414	G	T	15	GENIC	possibly homozygous	50158630