chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
16	20299914	20299915	A	G	48	GENIC	homozygous	111752480
16	20301050	20301051	A	G	48	GENIC	homozygous	111752484
16	20301234	20301235	T	A	39	GENIC	homozygous	111752486
16	20302564	20302565	T	C	35	GENIC	homozygous	111752494
16	20303113	20303122	AATTAATTA		38	GENIC	homozygous	131744785
16	20303698	20303699	A	G	35	GENIC	homozygous	111752498
16	20304036	20304037	A	G	30	GENIC	homozygous	111752500
16	20304163	20304164	T	C	45	GENIC	homozygous	111752502
16	20305305	20305306	T	A	57	GENIC	possibly homozygous	111752504
16	20303590	20303591	C	T	38	GENIC	homozygous	111948456
16	20304382	20304383	C	G	46	GENIC	homozygous	111948458
16	20304511	20304512	G	A	36	GENIC	homozygous	111948460
16	20304824	20304825	C	T	47	GENIC	homozygous	111948462
16	20305282	20305283	G	A	60	GENIC	homozygous	111948464
16	20303961	20303962	T	C	36	GENIC	homozygous	112130273
16	20304860	20304861	G	A	49	GENIC	homozygous	112107979
16	20306444	20306445	G	T	37	GENIC	homozygous	111948466
16	20306500	20306501	T	C	40	GENIC	possibly homozygous	111752506
16	20306852	20306853	C	G	36	GENIC	homozygous	111752508
16	20307042	20307043	G	A	38	GENIC	homozygous	111752510