chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
1	217019927	217019928	G	GGTGGT	9	INTERGENIC	possibly homozygous	61083912
1	217019966	217019967	T	C	9	INTERGENIC	homozygous	61925456
1	217021337	217021338	A	G	15	INTERGENIC	homozygous	61805052
1	217021410	217021411	G	A	21	INTERGENIC	possibly homozygous	61925457
1	217021913	217021914	G	T	10	INTERGENIC	possibly homozygous	61805054
1	217022002	217022003	G	-	4	INTERGENIC	homozygous	61925458
1	217022004	217022005	G	T	4	INTERGENIC	homozygous	62100230
1	217022016	217022017	T	C	2	INTERGENIC	homozygous	61805055
1	217022020	217022021	A	G	2	INTERGENIC	homozygous	61805056
1	217022054	217022055	T	C	9	INTERGENIC	homozygous	61925459
1	217022097	217022098	T	C	21	INTERGENIC	homozygous	61925460
1	217022575	217022576	G	A	13	INTERGENIC	possibly homozygous	62100231
1	217022576	217022577	A	C	12	INTERGENIC	possibly homozygous	62302531
1	217022609	217022610	C	G	25	INTERGENIC	homozygous	61925461
1	217023061	217023062	A	AAGACGT	8	INTERGENIC	homozygous	61805065
1	217023399	217023400	A	C	17	INTERGENIC	homozygous	61925462
1	217023536	217023537	T	C	18	INTERGENIC	homozygous	61925463
1	217023736	217023737	T	C	13	INTERGENIC	homozygous	61925464
1	217023765	217023766	G	GGGGA	2	INTERGENIC	heterozygous	61925465
1	217028402	217028403	T	C	21	INTERGENIC	possibly homozygous	61805085
1	217029096	217029098	AC	--	11	INTERGENIC	homozygous	61925466
1	217029395	217029396	T	C	13	INTERGENIC	possibly homozygous	61805092
1	217030471	217030472	T	C	19	INTERGENIC	homozygous	61805095
1	217031456	217031457	C	T	4	INTERGENIC	homozygous	61925467
1	217032628	217032629	A	C	9	INTERGENIC	homozygous	61925468
1	217032846	217032847	T	C	24	INTERGENIC	homozygous	61083937
1	217033863	217033864	G	GAA	1	INTERGENIC	homozygous	61083938