chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
1	66845089	66845090	C	G	13	GENIC	homozygous	147915439
1	66845483	66845491	GTGTGCGT		22	GENIC	homozygous	147891502
1	66846674	66846675	A	C	20	GENIC	homozygous	147915440
1	66847656	66847657	A	C	28	GENIC	homozygous	147915441
1	66847964	66847964		A	15	GENIC	possibly homozygous	147891503
1	66849278	66849279	C	G	9	GENIC	homozygous	147915442
1	66850696	66850697	T		15	GENIC	homozygous	147891504
1	66851140	66851140		G	2	GENIC	homozygous	147891505
1	66851339	66851340	T	C	16	GENIC	homozygous	147915443
1	66851732	66851733	C	T	22	GENIC	homozygous	147915444
1	66851976	66851977	T	C	14	GENIC	homozygous	147915445
1	66852424	66852425	G	A	16	GENIC	homozygous	147915446
1	66853003	66853004	T	C	8	GENIC	homozygous	147915447
1	66853085	66853086	G	A	14	GENIC	homozygous	147915448
1	66854381	66854382	T	G	20	GENIC	homozygous	147915449
1	66854498	66854499	A	G	14	GENIC	homozygous	147915450
1	66854522	66854523	C	T	13	GENIC	homozygous	147915451
1	66855304	66855305	A	G	19	GENIC	homozygous	147915452
1	66855745	66855746	G	T	8	GENIC	homozygous	147915453
1	66857164	66857165	A	G	17	GENIC	homozygous	147915454
1	66857322	66857323	G	A	14	GENIC	homozygous	147915455
1	66858602	66858603	C	T	15	GENIC	homozygous	147915456
1	66862840	66862840		GTATGACT	9	GENIC	homozygous	147891506
1	66864134	66864135	T	G	20	GENIC	homozygous	147915461
1	66859779	66859780	G	A	13	GENIC	homozygous	147915457
1	66860582	66860583	G	A	18	GENIC	homozygous	147915458
1	66861331	66861332	G	A	17	GENIC	homozygous	147915459
1	66863041	66863042	T	C	16	GENIC	homozygous	147915460
1	66864321	66864322	A	T	12	GENIC	homozygous	147915462