chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
4	146430520	146430521	T	A	28	GENIC	homozygous	146424234
4	146433501	146433502	G	A	22	GENIC	possibly homozygous	137226273
4	146433704	146433705	C	A	19	GENIC	homozygous	137226274
4	146435299	146435300	T	C	15	GENIC	homozygous	137226275
4	146435860	146435861	C	G	19	GENIC	homozygous	137226276
4	146436080	146436081	T	C	16	GENIC	homozygous	146424235
4	146436525	146436526	T	A	16	GENIC	homozygous	146424236
4	146437146	146437147	G	T	14	GENIC	homozygous	137226277
4	146439509	146439510	A	C	20	GENIC	homozygous	137226278
4	146440003	146440004	T	C	16	GENIC	homozygous	146424237
4	146441737	146441738	T	C	20	GENIC	homozygous	146424238
4	146442699	146442700	T	C	30	GENIC	homozygous	137226280
4	146445751	146445752	C	T	18	GENIC	homozygous	146424239
4	146450658	146450659	A	G	10	GENIC	homozygous	137226281
4	146451214	146451215	A	G	21	GENIC	homozygous	137226282
4	146451502	146451503	A	T	18	GENIC	homozygous	146424240
4	146439673	146439674	G	A	17	GENIC	homozygous	403122326
4	146439673	146439674	G		17	GENIC	heterozygous	403122325
4	146449067	146449068	A		27	GENIC	homozygous	146403729
4	146434658	146434662	ATTT		12	GENIC	homozygous	146403727