chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
1	219099122	219099123	A	AG	12	GENIC	homozygous	62588768
1	219099213	219099214	A	G	32	GENIC	homozygous	61593499
1	219104584	219104585	T	C	19	GENIC	homozygous	61593500
1	219105445	219105446	C	T	25	GENIC	homozygous	62588769
1	219105557	219105558	C	T	37	GENIC	possibly homozygous	62588770
1	219107532	219107533	A	AG	21	GENIC	heterozygous	61593503
1	219107532	219107533	A	AGG	21	GENIC	possibly homozygous	62588771
1	219109999	219110000	T	C	28	GENIC	homozygous	61593511
1	219112584	219112585	C	CA	13	GENIC	heterozygous	62697214
1	219114307	219114308	A	G	26	GENIC	homozygous	61593528
1	219114367	219114368	A	G	28	GENIC	homozygous	62588772
1	219115389	219115390	A	G	27	GENIC	homozygous	62588773
1	219117357	219117358	A	G	24	GENIC	homozygous	62588774
1	219120881	219120887	CTCTCG	------	22	GENIC	heterozygous	62414127
1	219122530	219122531	A	ATG	15	GENIC	heterozygous	61089416
1	219122574	219122575	G	GTGTGTGTGT	26	GENIC	heterozygous	62236913
1	219126483	219126484	G	-	17	GENIC	homozygous	62414129
1	219126486	219126489	TGG	---	18	GENIC	homozygous	62414131
1	219126492	219126493	G	T	17	GENIC	homozygous	62588775
1	219126496	219126497	G	T	17	GENIC	homozygous	62588776
1	219126500	219126501	G	T	18	GENIC	homozygous	62588777
1	219126651	219126652	A	AGTTG	9	GENIC	homozygous	62588778
1	219129721	219129722	C	CAA	18	GENIC	homozygous	61593578
1	219127277	219127278	T	G	27	GENIC	possibly homozygous	61593570
1	219128314	219128315	T	C	38	GENIC	homozygous	61593574
1	219127029	219127033	CTCT	----	6	GENIC	heterozygous	62199339
1	219130308	219130309	C	CA	38	GENIC	homozygous	61593579
1	219131620	219131621	A	T	34	GENIC	homozygous	62588779
1	219132609	219132610	T	G	39	GENIC	homozygous	61593581
1	219134122	219134126	ACAC	----	12	GENIC	homozygous	62199341