chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
1	171006637	171006638	A	AG	21	GENIC	homozygous	60941889
1	171006649	171006650	A	AG	19	GENIC	homozygous	60941891
1	171006679	171006680	A	AG	9	GENIC	possibly homozygous	60941894
1	171006679	171006680	A	AAGG	9	GENIC	heterozygous	62173535
1	171006682	171006683	A	AGGGAAGGGAAG	9	GENIC	heterozygous	62173537
1	171006682	171006683	A	AGGGAAGGGAAGGGAAGGGAAGGGAAGGGAAGGGAAG	9	GENIC	possibly homozygous	62271412
1	171008278	171008279	C	CAA	10	GENIC	possibly homozygous	61555235
1	171009510	171009511	T	TAA	13	GENIC	homozygous	61555236
1	171009879	171009880	G	A	12	GENIC	homozygous	61555238
1	171009885	171009886	C	T	15	GENIC	possibly homozygous	61555239
1	171009908	171009909	G	GA	12	GENIC	homozygous	60941899
1	171010471	171010474	AAA	---	9	GENIC	heterozygous	62271413
1	171010794	171010795	C	T	31	GENIC	homozygous	61555240
1	171011120	171011121	C	T	22	GENIC	homozygous	61555241
1	171011885	171011886	C	T	21	GENIC	homozygous	61555242
1	171012238	171012239	A	G	21	GENIC	homozygous	61555243
1	171013099	171013100	A	AG	21	GENIC	homozygous	61555244
1	171013457	171013458	T	TA	12	GENIC	possibly homozygous	61555245
1	171013457	171013458	T	TAAAAA	12	GENIC	heterozygous	61555246
1	171013701	171013702	G	A	30	GENIC	homozygous	61555247
1	171014231	171014232	A	G	20	GENIC	homozygous	61555248
1	171014391	171014392	T	C	26	GENIC	homozygous	61555249
1	171014858	171014859	C	T	26	GENIC	homozygous	61555250
1	171015885	171015886	C	T	21	GENIC	homozygous	61555251
1	171015996	171015997	C	CTAAA	25	GENIC	homozygous	61555252
1	171016250	171016251	T	C	21	GENIC	homozygous	61555253
1	171016464	171016465	C	T	14	GENIC	homozygous	61555254