chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
12	50030236	50030237	A	G	21	GENIC	homozygous	50235932
12	50030283	50030284	G	A	38	GENIC	homozygous	50235934
12	50030872	50030873	C	T	22	GENIC	homozygous	50235936
12	50031119	50031120	T	C	19	GENIC	homozygous	50235940
12	50031259	50031260	T	TGCGCAC	16	GENIC	homozygous	50235942
12	50031303	50031304	C	T	32	GENIC	homozygous	50235944
12	50031730	50031731	T	C	13	GENIC	homozygous	50235946
12	50031937	50031938	C	T	20	GENIC	homozygous	50235950
12	50032399	50032400	G	A	26	GENIC	homozygous	50235952
12	50032789	50032790	G	A	29	GENIC	homozygous	50235954
12	50033186	50033187	G	A	32	GENIC	homozygous	50235956
12	50033747	50033748	A	AC	19	GENIC	possibly homozygous	50546808
12	50033748	50033749	A	C	19	GENIC	possibly homozygous	50546809
12	50033760	50033765	AAAAC	-----	18	GENIC	homozygous	50235960
12	50033921	50033922	G	C	28	GENIC	homozygous	50235964
12	50034291	50034292	G	A	20	GENIC	homozygous	50235966
12	50034376	50034377	A	G	14	GENIC	homozygous	50235968
12	50034428	50034431	AAG	---	6	GENIC	heterozygous	50235970
12	50034755	50034756	A	T	41	GENIC	homozygous	50235974
12	50035056	50035057	C	T	20	GENIC	homozygous	50235976
12	50035299	50035300	T	TA	10	GENIC	possibly homozygous	50235978
12	50036205	50036206	A	C	21	GENIC	homozygous	50235980
12	50036800	50036801	G	A	14	GENIC	homozygous	50235984