chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
1	225908011	225908012	T	G	13	GENIC	homozygous	108558194
1	225914910	225914911	T	G	77	GENIC	heterozygous	108771837
1	225922751	225922752	C	T	23	GENIC	homozygous	108997435
1	225977273	225977274	A	C	83	GENIC	heterozygous	108558333
1	225977316	225977317	C	T	77	GENIC	heterozygous	108771845
1	225977317	225977318	A	G	76	GENIC	heterozygous	108558334
1	225986118	225986119	A	G	20	GENIC	possibly homozygous	109198201
1	226015698	226015699	G	T	58	GENIC	heterozygous	109198203
1	226015724	226015725	G	A	58	GENIC	heterozygous	109198205
1	226015729	226015730	T	A	59	GENIC	heterozygous	108771848
1	226015740	226015741	T	A	54	GENIC	heterozygous	109198207
1	226053947	226053948	A	T	6	GENIC	homozygous	108558501
1	226078692	226078693	A	G	31	GENIC	heterozygous	109198209
1	226099668	226099669	G	A	25	GENIC	heterozygous	108558543
1	226129471	226129472	A	T	14	GENIC	homozygous	108558544
1	226129485	226129486	A	T	20	GENIC	homozygous	108558545
1	226129500	226129501	T	C	18	GENIC	homozygous	108558546
1	226129565	226129566	A	T	25	GENIC	possibly homozygous	108558547
1	226129568	226129569	T	G	24	GENIC	homozygous	109198211
1	226129716	226129717	C	G	36	GENIC	homozygous	108558548
1	226131591	226131592	A	C	9	GENIC	homozygous	108558549