chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
10	36079697	36079698	A	G	30	GENIC	homozygous	51411309
10	36080066	36080067	A	G	21	GENIC	homozygous	51411313
10	36080119	36080120	G	C	24	GENIC	homozygous	51411315
10	36080573	36080574	A	G	23	GENIC	homozygous	51848965
10	36080959	36080960	T	C	36	GENIC	homozygous	51411321
10	36086206	36086207	G	GA	20	GENIC	possibly homozygous	52039183
10	36086830	36086831	C	T	10	GENIC	homozygous	52241095
10	36086947	36086948	T	C	31	GENIC	homozygous	51411375
10	36087304	36087305	G	A	38	GENIC	homozygous	52302422
10	36087459	36087460	G	A	29	GENIC	homozygous	52302424
10	36088515	36088516	T	TC	7	GENIC	homozygous	52302426
10	36088695	36088696	T	C	14	GENIC	homozygous	51411391
10	36090779	36090780	A	-	22	GENIC	homozygous	52302428
10	36091947	36091948	G	A	21	GENIC	homozygous	52039187
10	36091976	36091977	C	T	15	GENIC	homozygous	52302430
10	36091988	36091989	G	T	15	GENIC	homozygous	52302432
10	36091995	36091996	A	AGCT	18	GENIC	homozygous	51411430
10	36092005	36092006	T	A	18	GENIC	homozygous	52302434
10	36092015	36092016	C	T	17	GENIC	homozygous	52302436
10	36092142	36092143	C	T	19	GENIC	homozygous	51411434
10	36092244	36092245	G	A	23	GENIC	homozygous	52302438
10	36092284	36092285	T	C	21	GENIC	homozygous	52302440
10	36092374	36092375	T	C	13	GENIC	homozygous	52039189
10	36092474	36092475	T	C	17	GENIC	homozygous	51411436
10	36092596	36092597	T	A	10	GENIC	homozygous	51411438
10	36092770	36092771	C	G	14	GENIC	homozygous	51411440
10	36092863	36092864	C	T	21	GENIC	homozygous	51411442
10	36092927	36092928	A	G	16	GENIC	homozygous	51411444
10	36092941	36092942	C	T	15	GENIC	homozygous	51411446
10	36093071	36093072	A	G	16	GENIC	homozygous	51411448
10	36093112	36093113	T	C	22	GENIC	homozygous	51411450
10	36093765	36093766	T	A	11	GENIC	homozygous	51411452
10	36093850	36093851	C	G	28	GENIC	homozygous	51411454
10	36094012	36094013	G	T	23	GENIC	homozygous	51411456
10	36094178	36094187	CATCTGCAC	---------	23	GENIC	homozygous	51411458