chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
18	60853480	60853481	G	A	17	GENIC	homozygous	46689558
18	60854391	60854392	C	A	32	GENIC	homozygous	46689559
18	60854407	60854408	C	T	34	GENIC	homozygous	46689560
18	60855557	60855558	T	G	26	GENIC	homozygous	46480463
18	60856438	60856439	G	A	33	GENIC	homozygous	46689561
18	60857425	60857426	T	TCTCTCTCTCTCTCTCTCTCTCTCTCC	15	GENIC	homozygous	46819153
18	60858385	60858386	T	C	30	GENIC	homozygous	46480467
18	60858934	60858935	C	T	32	GENIC	homozygous	46689562
18	60859471	60859473	TA	--	22	GENIC	homozygous	46480482
18	60860133	60860134	G	A	22	GENIC	homozygous	46689563
18	60861233	60861234	G	A	29	GENIC	homozygous	46689564
18	60861305	60861306	G	A	23	GENIC	homozygous	46689565
18	60861569	60861570	T	-	17	GENIC	possibly homozygous	46666192
18	60861717	60861718	C	T	26	GENIC	homozygous	46689566
18	60861784	60861785	G	A	23	GENIC	homozygous	46689567
18	60861813	60861814	G	A	26	GENIC	homozygous	46689568
18	60862065	60862066	T	C	27	GENIC	homozygous	46480492
18	60862597	60862598	G	GCA	29	GENIC	homozygous	46689569
18	60862660	60862661	T	C	40	GENIC	homozygous	46666194
18	60864395	60864396	G	C	21	GENIC	homozygous	46689570
18	60865549	60865550	C	T	17	GENIC	homozygous	46689571
18	60865881	60865882	T	G	25	GENIC	homozygous	46480500
18	60865885	60865886	G	T	25	GENIC	homozygous	46480501
18	60865929	60865930	A	AGTCT	23	GENIC	homozygous	46480502
18	60866172	60866173	G	A	30	GENIC	homozygous	46480504
18	60867345	60867346	G	GTT	7	GENIC	homozygous	46480508
18	60867715	60867716	T	C	19	GENIC	homozygous	46480509