chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
2	219702971	219702972	A	G	25	GENIC	homozygous	74369545
2	219703197	219703198	C	T	26	GENIC	homozygous	74369548
2	219704178	219704179	T	C	24	GENIC	homozygous	74369550
2	219705406	219705407	T	C	3	GENIC	homozygous	74369559
2	219711987	219711988	A	T	32	GENIC	homozygous	74369565
2	219714916	219714917	C	T	26	GENIC	homozygous	74369568
2	219715289	219715290	A	G	22	GENIC	homozygous	74369571
2	219715832	219715833	C	T	25	GENIC	homozygous	74369574
2	219716781	219716782	C	A	30	GENIC	homozygous	74369577
2	219717381	219717382	T	A	12	GENIC	homozygous	74369580
2	219717411	219717412	A	G	16	GENIC	homozygous	74369583
2	219717754	219717755	T	A	22	GENIC	homozygous	74369586
2	219718521	219718522	T	G	8	GENIC	possibly homozygous	74369589
2	219718956	219718957	G	C	27	GENIC	homozygous	74369592
2	219718987	219718988	C	T	28	GENIC	homozygous	74369595
2	219719078	219719079	C	T	22	GENIC	homozygous	74369598
2	219720180	219720181	G	A	22	GENIC	homozygous	74369601
2	219723110	219723111	G	A	10	GENIC	heterozygous	75630607
2	219721102	219721103	G	T	10	GENIC	homozygous	74369604
2	219721219	219721220	G	A	27	GENIC	homozygous	74369607
2	219707216	219707217	T	A	18	GENIC	homozygous	75630604
2	219720465	219720466	A	C	22	GENIC	possibly homozygous	75630605
2	219723108	219723109	G	A	10	GENIC	heterozygous	75630606
2	219723319	219723320	A	G	38	GENIC	homozygous	74369610
2	219723683	219723684	T	C	36	GENIC	homozygous	74369613
2	219723962	219723963	C	T	25	GENIC	homozygous	74369616
2	219724644	219724645	C	T	15	GENIC	homozygous	74369619
2	219724854	219724855	G	C	26	GENIC	homozygous	74369622