chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
2	219599582	219599583	C	T	38	GENIC	homozygous	110824098
2	219599602	219599603	T	C	45	GENIC	homozygous	110824099
2	219600990	219600991	G	T	32	GENIC	homozygous	110824100
2	219601225	219601226	T	G	25	GENIC	homozygous	110824101
2	219601496	219601497	C	T	26	GENIC	homozygous	110824102
2	219602502	219602503	C	T	36	GENIC	homozygous	110824106
2	219602739	219602740	T	C	39	GENIC	homozygous	110249303
2	219603152	219603153	G	A	31	GENIC	homozygous	110249305
2	219603709	219603710	T	C	40	GENIC	homozygous	110824107
2	219603905	219603906	T	C	39	GENIC	homozygous	110249307
2	219603920	219603921	G	A	41	GENIC	homozygous	110249309
2	219603969	219603970	G	A	26	GENIC	homozygous	110249311
2	219604126	219604127	C	T	23	GENIC	homozygous	110249313
2	219605234	219605235	T	C	15	GENIC	homozygous	110249315
2	219607732	219607733	T	C	23	GENIC	homozygous	110249317
2	219609658	219609659	G	A	31	GENIC	homozygous	110824108
2	219609879	219609880	G	C	15	GENIC	homozygous	110824109
2	219609972	219609973	A	G	57	GENIC	homozygous	110249325
2	219611405	219611406	T	C	44	GENIC	homozygous	110249328
2	219611632	219611633	G	A	49	GENIC	homozygous	110249330
2	219616690	219616691	A	G	91	GENIC	homozygous	110824112
2	219616915	219616916	A	C	64	GENIC	homozygous	110824113