chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
10	85594342	85594343	G	-	24	GENIC	homozygous	51526323
10	85594433	85594434	G	T	22	GENIC	homozygous	51526325
10	85594436	85594437	T	TC	20	GENIC	homozygous	51526326
10	85594445	85594446	G	T	20	GENIC	homozygous	51526327
10	85596191	85596192	C	CT	6	GENIC	heterozygous	51526329
10	85597886	85597887	T	-	3	GENIC	heterozygous	52731559
10	85598336	85598337	G	T	9	GENIC	homozygous	51526334
10	85606153	85606154	C	CA	28	GENIC	homozygous	51526348
10	85606181	85606182	A	AC	29	GENIC	homozygous	51526349
10	85609799	85609800	A	G	24	GENIC	possibly homozygous	51526359
10	85610621	85610625	TTAT	----	6	GENIC	homozygous	51526362
10	85614749	85614750	C	CA	9	GENIC	heterozygous	51526371
10	85614750	85614751	A	-	9	GENIC	heterozygous	51526372
10	85606289	85606290	G	GCTC	15	GENIC	homozygous	52392157
10	85606283	85606284	T	TGCTTGCTAGG	16	GENIC	homozygous	52392155