chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
12	4733282	4733283	C	T	29	GENIC	homozygous	50005005
12	4733633	4733634	T	C	24	GENIC	homozygous	50395059
12	4733678	4733679	T	C	24	GENIC	homozygous	50395061
12	4733844	4733845	T	G	26	GENIC	homozygous	50005007
12	4735038	4735039	C	T	26	GENIC	homozygous	50395063
12	4735421	4735422	T	G	45	GENIC	homozygous	50395065
12	4736471	4736472	T	G	13	GENIC	homozygous	50005008
12	4736582	4736583	T	C	23	GENIC	homozygous	50395067
12	4736830	4736838	TTATTTAT	--------	9	GENIC	homozygous	50395069
12	4736837	4736838	T	-	15	GENIC	heterozygous	50395071
12	4737911	4737912	G	T	31	GENIC	homozygous	50395072
12	4739264	4739265	T	C	22	GENIC	homozygous	50395074
12	4739392	4739393	C	CTT	26	GENIC	homozygous	50005014
12	4739445	4739446	G	T	32	GENIC	homozygous	50005016
12	4739594	4739595	G	T	23	GENIC	homozygous	50005018
12	4739607	4739608	A	ATTT	17	GENIC	homozygous	50005020
12	4739613	4739614	G	T	20	GENIC	possibly homozygous	50005022
12	4739613	4739614	G	GCT	19	GENIC	heterozygous	50005024
12	4739616	4739617	G	GCT	18	GENIC	homozygous	50005026
12	4739631	4739632	G	A	18	GENIC	homozygous	50005028
12	4739653	4739654	G	T	20	GENIC	homozygous	50005030
12	4739705	4739706	C	A	30	GENIC	homozygous	50005032