chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
10	72669130	72669131	G	A	18	GENIC	homozygous	138817321
10	72670330	72670331	A	G	23	GENIC	homozygous	138817322
10	72671378	72671379	C		30	GENIC	homozygous	138690563
10	72671634	72671635	C	T	25	GENIC	homozygous	138817323
10	72671642	72671643	C	T	24	GENIC	homozygous	138817324
10	72671995	72671995		G	23	GENIC	homozygous	138690564
10	72672458	72672459	A	C	11	GENIC	possibly homozygous	138817325
10	72672621	72672622	G	A	22	GENIC	homozygous	138817326
10	72673188	72673189	C	T	18	GENIC	homozygous	138817327
10	72673391	72673392	G	T	26	GENIC	homozygous	138817328
10	72673406	72673407	T	C	27	GENIC	homozygous	138817329
10	72674344	72674345	T	C	8	GENIC	homozygous	138817330
10	72674371	72674372	G	C	7	GENIC	homozygous	138817331
10	72674814	72674815	G	A	11	GENIC	homozygous	138817332
10	72676054	72676055	A	G	10	GENIC	homozygous	138817333
10	72677073	72677074	G	T	15	GENIC	homozygous	138817334
10	72677379	72677380	A	G	17	GENIC	homozygous	138817335