chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
2	164747850	164747851	C	T	15	GENIC	homozygous	110111226
2	164748900	164748901	A	T	45	GENIC	homozygous	110111227
2	164748994	164748995	C	T	38	GENIC	homozygous	110111228
2	164750143	164750144	G	A	43	GENIC	homozygous	110111229
2	164753243	164753244	A	G	27	GENIC	homozygous	110111230
2	164753733	164753734	A	G	19	GENIC	homozygous	110111231
2	164753768	164753769	A	G	21	GENIC	homozygous	110111232
2	164754353	164754354	G	A	44	GENIC	homozygous	110111233
2	164755353	164755354	A	T	33	GENIC	homozygous	110111234
2	164755782	164755783	G	T	37	GENIC	possibly homozygous	110111235
2	164756526	164756527	C	T	28	GENIC	homozygous	110111236
2	164757293	164757294	A	G	22	GENIC	homozygous	110111239
2	164758460	164758461	T	C	33	GENIC	homozygous	110111240
2	164760133	164760134	G	A	44	GENIC	homozygous	110111241
2	164761039	164761040	C	T	45	GENIC	homozygous	110111242
2	164761102	164761103	A	G	33	GENIC	homozygous	110111243
2	164761888	164761889	A	G	27	GENIC	homozygous	110111244
2	164763640	164763641	G	A	39	GENIC	homozygous	110111245
2	164766059	164766060	T	C	33	GENIC	homozygous	110111246
2	164766078	164766079	C	T	30	GENIC	homozygous	110111247