chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
12	14206203	14206204	A	T	42	GENIC	homozygous	139089109
12	14206303	14206304	C	T	39	GENIC	homozygous	139089110
12	14207225	14207226	G	A	35	GENIC	homozygous	139089111
12	14208162	14208163	G	T	25	GENIC	homozygous	154748311
12	14208162	14208163	G		25	GENIC	heterozygous	403317417
12	14209186	14209187	G	T	39	GENIC	homozygous	139089112
12	14210332	14210333	C		5	GENIC	homozygous	403317418
12	14210332	14210333	C	A	5	GENIC	heterozygous	403317419
12	14210335	14210336	C		5	GENIC	homozygous	403317420
12	14210335	14210336	C	A	5	GENIC	heterozygous	403317421
12	14210338	14210339	C	A	5	GENIC	heterozygous	403317422
12	14210338	14210339	C		5	GENIC	homozygous	403317423
12	14215506	14215507	G	C	38	GENIC	homozygous	139089113
12	14215702	14215703	A	G	16	GENIC	heterozygous	139089114
12	14216963	14216964	A	C	33	GENIC	homozygous	139089115
12	14218707	14218708	C	A	42	GENIC	homozygous	139089116
12	14218991	14218995	AAAC		36	GENIC	homozygous	139042102
12	14215299	14215299		TTC	41	GENIC	homozygous	139042100
12	14215688	14215694	GCACAC		14	GENIC	possibly homozygous	139042101