chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
1	107917447	107917448	C	T	41	GENIC	homozygous	61739580
1	107922010	107922012	AC	--	9	GENIC	heterozygous	61299895
1	107923049	107923051	GC	--	27	GENIC	heterozygous	60783214
1	107924401	107924402	A	AT	45	GENIC	homozygous	60783220
1	107978875	107978876	G	A	23	GENIC	homozygous	60783300
1	107980649	107980650	A	T	16	GENIC	homozygous	60783303
1	107980707	107980708	A	AG	22	GENIC	homozygous	60783305
1	107983584	107983585	T	G	61	GENIC	heterozygous	61739582
1	107983653	107983654	G	T	71	GENIC	heterozygous	61739584
1	107983770	107983771	G	A	50	GENIC	heterozygous	60783318
1	107984981	107984982	C	T	70	GENIC	heterozygous	60783323
1	107984998	107984999	G	A	70	GENIC	heterozygous	60783324
1	107985005	107985006	C	T	70	GENIC	heterozygous	60783325
1	107985044	107985045	T	C	54	GENIC	heterozygous	60783326
1	107992489	107992490	T	TGATA	36	GENIC	possibly homozygous	60783348
1	107992535	107992536	A	ATAGG	63	GENIC	heterozygous	61671129
1	107998910	107998912	CA	--	11	GENIC	homozygous	61497239
1	108002234	108002235	A	G	42	GENIC	homozygous	60783385