chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
16	37177512	37177513	A	T	25	GENIC	homozygous	111972004
16	37177585	37177586	G	A	22	GENIC	homozygous	112154509
16	37178406	37178407	G	A	21	GENIC	homozygous	111972008
16	37178653	37178654	G	T	15	GENIC	possibly homozygous	111972010
16	37181075	37181076	T	G	9	GENIC	possibly homozygous	111972012
16	37181079	37181080	G	C	9	GENIC	possibly homozygous	111972014
16	37181126	37181127	T	G	10	GENIC	homozygous	111972016
16	37181572	37181573	G	A	21	GENIC	possibly homozygous	112154512
16	37181706	37181707	G	A	28	GENIC	possibly homozygous	112154514
16	37181932	37181933	G	A	27	GENIC	possibly homozygous	112154516
16	37184567	37184568	A	G	30	GENIC	homozygous	111972022
16	37186088	37186089	C	T	24	GENIC	homozygous	112154518
16	37186439	37186440	A	T	32	GENIC	possibly homozygous	112154520
16	37188086	37188087	T	C	23	GENIC	possibly homozygous	112154522
16	37191072	37191073	C	T	18	GENIC	homozygous	112154524
16	37192569	37192570	G	T	25	GENIC	heterozygous	111972034
16	37192836	37192837	T	G	20	GENIC	possibly homozygous	111972036
16	37194308	37194309	G	T	3	GENIC	homozygous	112154526
16	37194368	37194369	C	A	4	GENIC	homozygous	112154528
16	37194955	37194956	G	A	23	GENIC	homozygous	112154530
16	37195615	37195616	A	G	21	GENIC	homozygous	111972042
16	37197933	37197934	C	G	32	GENIC	homozygous	111972046
16	37181114	37181115	C	T	10	GENIC	homozygous	112405454
16	37190674	37190675	A	C	9	GENIC	homozygous	111781989
16	37190676	37190677	C	T	9	GENIC	homozygous	111781991