chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
20	39612140	39612141	A	G	17	GENIC	homozygous	45555299
20	39612302	39612303	T	TAAA	19	GENIC	possibly homozygous	45555300
20	39612302	39612303	T	TAA	19	GENIC	heterozygous	45891653
20	39612532	39612533	C	T	24	GENIC	homozygous	45555301
20	39612936	39612937	T	-	3	GENIC	heterozygous	45555304
20	39613149	39613150	C	-	1	GENIC	homozygous	45555305
20	39613419	39613420	G	GTTT	3	GENIC	heterozygous	45555306
20	39613419	39613420	G	GTT	3	GENIC	heterozygous	45555307
20	39614109	39614110	C	A	14	GENIC	homozygous	45555309
20	39616337	39616338	C	T	26	GENIC	homozygous	45555310
20	39620276	39620277	G	T	20	GENIC	homozygous	45989836
20	39622774	39622775	G	A	16	GENIC	homozygous	45989838
20	39623235	39623236	A	-	2	GENIC	homozygous	45555311
20	39623536	39623537	G	GTTT	15	GENIC	heterozygous	45555312
20	39623536	39623537	G	GTT	15	GENIC	heterozygous	45822763
20	39624105	39624106	A	AT	17	GENIC	homozygous	45822764
20	39624314	39624315	A	AAAAAC	28	GENIC	homozygous	45989840
20	39624339	39624340	A	G	29	GENIC	homozygous	45555315
20	39624495	39624496	T	A	29	GENIC	homozygous	45555316