chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
4	155681820	155681821	T	TA	12	GENIC	homozygous	58089381
4	155683619	155683620	G	C	16	GENIC	homozygous	58089383
4	155683941	155683942	C	CGGG	13	GENIC	homozygous	58089385
4	155685385	155685386	G	T	19	GENIC	homozygous	58089389
4	155686017	155686018	A	G	19	GENIC	homozygous	57526714
4	155686660	155686661	A	T	25	GENIC	homozygous	58089391
4	155687107	155687108	T	G	17	GENIC	homozygous	58089393
4	155688536	155688537	G	GTTTT	21	GENIC	homozygous	57526724
4	155688620	155688621	G	A	36	GENIC	homozygous	58089395
4	155688894	155688899	GGTTC	-----	30	GENIC	homozygous	57526730
4	155688958	155688959	G	C	41	GENIC	homozygous	58089397
4	155689322	155689323	A	C	15	GENIC	homozygous	57526740
4	155690734	155690735	C	G	24	INTERGENIC	homozygous	58089399
4	155690760	155690761	C	T	30	INTERGENIC	homozygous	58089401
4	155691021	155691022	T	-	23	INTERGENIC	homozygous	58089403
4	155684127	155684128	G	GAGAGACAGACAGAGAGAGAGAC	13	GENIC	heterozygous	58348311
4	155688537	155688538	G	T	21	GENIC	homozygous	58348313
4	155689324	155689325	A	AT	1	GENIC	homozygous	58348315
4	155688566	155688567	G	GTTA	36	GENIC	possibly homozygous	58287271