chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
3	86649542	86649543	T	C	15	GENIC	homozygous	57527545
3	86650158	86650159	T	G	20	GENIC	homozygous	57527547
3	86650446	86650447	A	G	9	GENIC	heterozygous	57527549
3	86651553	86651554	C	T	31	GENIC	possibly homozygous	57527551
3	86652159	86652160	T	C	31	GENIC	homozygous	57527561
3	86652641	86652642	A	G	3	GENIC	heterozygous	57527563
3	86652700	86652701	A	G	22	GENIC	homozygous	57527565
3	86652925	86652926	G	A	19	GENIC	homozygous	57527567
3	86653569	86653570	C	T	15	GENIC	homozygous	57527573
3	86654204	86654205	T	C	20	GENIC	homozygous	57527575
3	86657171	86657172	T	TGTGC	2	GENIC	homozygous	57527581
3	86657749	86657750	T	TTCC	6	GENIC	homozygous	57527585
3	86657759	86657760	A	G	13	GENIC	possibly homozygous	57527587
3	86658347	86658348	T	C	7	GENIC	heterozygous	57527593
3	86658848	86658849	G	A	15	GENIC	possibly homozygous	58470330
3	86659012	86659013	G	A	22	GENIC	heterozygous	57527595
3	86659886	86659887	G	C	21	GENIC	possibly homozygous	57527597
3	86659992	86659993	G	A	9	GENIC	homozygous	57527601
3	86660136	86660137	T	C	20	GENIC	possibly homozygous	57527603
3	86660646	86660647	C	CCA	3	GENIC	homozygous	57527605
3	86660775	86660776	G	A	14	GENIC	heterozygous	57527607
3	86660861	86660862	G	A	21	GENIC	possibly homozygous	57527609
3	86661046	86661049	AAA	---	7	GENIC	homozygous	57527611
3	86661398	86661399	C	T	19	GENIC	possibly homozygous	57527613
3	86661668	86661669	T	-	20	GENIC	homozygous	57527615
3	86663494	86663495	A	G	26	GENIC	homozygous	57527621
3	86663849	86663850	G	C	9	GENIC	possibly homozygous	58470332
3	86664060	86664061	A	AAGACG	4	GENIC	homozygous	57527625
3	86664728	86664729	T	C	28	GENIC	homozygous	57527627
3	86664974	86664975	A	AT	2	GENIC	homozygous	57527629
3	86666651	86666652	A	G	21	GENIC	possibly homozygous	57527631
3	86667031	86667032	A	G	28	GENIC	possibly homozygous	58470334