chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
2	219708504	219708505	T	C	28	GENIC	homozygous	110249481
2	219712394	219712395	G	A	31	GENIC	homozygous	111169642
2	219712650	219712651	C	T	22	GENIC	homozygous	111169644
2	219715410	219715411	T	C	23	GENIC	homozygous	110249489
2	219716985	219716986	T	G	22	GENIC	heterozygous	120254510
2	219717158	219717159	T	C	35	GENIC	homozygous	110249497
2	219717228	219717229	C	T	30	GENIC	homozygous	110249499
2	219718145	219718146	A	G	21	GENIC	homozygous	111169646
2	219718771	219718772	C	T	17	GENIC	homozygous	111169648
2	219719529	219719530	T	C	14	GENIC	homozygous	110824141
2	219717287	219717288	G	T	14	GENIC	heterozygous	120272694
2	219720769	219720770	T	C	19	GENIC	homozygous	111169650
2	219722356	219722357	C	T	36	GENIC	homozygous	111169652
2	219725041	219725042	T	C	21	GENIC	homozygous	110249517
2	219727419	219727420	C	T	23	GENIC	homozygous	111169658
2	219727656	219727657	C	G	24	GENIC	homozygous	110824145
2	219731615	219731616	G	A	22	GENIC	homozygous	110249533
2	219734261	219734262	C	A	34	GENIC	homozygous	110249539
2	219734284	219734285	C	T	31	GENIC	homozygous	110824146
2	219735318	219735319	C	T	30	GENIC	homozygous	111169660
2	219736932	219736933	A	G	11	GENIC	homozygous	110249543
2	219737386	219737387	A	G	37	GENIC	possibly homozygous	110249545
2	219740993	219740994	T	C	27	GENIC	homozygous	110249549