chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
10	85588984	85588985	G	A	22	GENIC	homozygous	52162965
10	85589155	85589156	A	G	25	GENIC	homozygous	51526308
10	85589207	85589208	A	G	20	GENIC	homozygous	51526311
10	85590153	85590154	G	T	12	GENIC	homozygous	52162966
10	85590707	85590708	A	AAAGTCTTAAGAGGGAGGAGGGGACGTTTAAGGGAGGAGTTTAAGGGAGGAGCTATGAGAGGGTG	12	GENIC	homozygous	52847851
10	85591539	85591540	T	-	7	GENIC	homozygous	51526318
10	85593386	85593390	TCTT	----	18	GENIC	homozygous	51526320
10	85593595	85593596	C	CTTCTT	7	GENIC	heterozygous	51526321
10	85593595	85593596	C	CTTCT	7	GENIC	possibly homozygous	52847854
10	85594342	85594343	G	-	20	GENIC	homozygous	51526323
10	85594406	85594407	T	TG	19	GENIC	homozygous	51526324
10	85594433	85594434	G	T	16	GENIC	homozygous	51526325
10	85594436	85594437	T	TC	18	GENIC	homozygous	51526326
10	85594445	85594446	G	T	17	GENIC	homozygous	51526327
10	85596191	85596192	C	CT	6	GENIC	homozygous	51526329
10	85596523	85596524	A	AT	3	GENIC	homozygous	51526332
10	85597885	85597886	C	CT	1	GENIC	homozygous	52847857
10	85598336	85598337	G	T	7	GENIC	homozygous	51526334
10	85602935	85602936	G	T	19	GENIC	homozygous	52162969
10	85605228	85605229	A	AAAGAAAGG	6	GENIC	homozygous	52847860
10	85606153	85606154	C	CA	30	GENIC	homozygous	51526348
10	85606181	85606182	A	AC	24	GENIC	homozygous	51526349
10	85606191	85606192	T	TA	21	GENIC	homozygous	52847863
10	85606283	85606284	T	TGCTTGCTAGG	15	GENIC	heterozygous	52392155
10	85606289	85606290	G	GCTC	7	GENIC	homozygous	52392157
10	85606995	85606996	C	T	25	GENIC	homozygous	51526354
10	85608019	85608020	T	-	12	GENIC	homozygous	52162970
10	85609799	85609800	A	G	15	GENIC	homozygous	51526359
10	85609802	85609803	C	-	16	GENIC	homozygous	51526360
10	85610483	85610484	G	-	14	GENIC	homozygous	52071596
10	85614749	85614750	C	CA	5	GENIC	heterozygous	51526371
10	85614750	85614751	A	-	5	GENIC	heterozygous	51526372
10	85616161	85616171	AACAAAACAA	----------	8	GENIC	homozygous	51526378
10	85616304	85616305	G	T	18	GENIC	homozygous	51526379