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	14	GENIC	homozygous	45555300
20	39612532	39612533	C	T	29	GENIC	homozygous	45555301
20	39612587	39612588	T	C	26	GENIC	homozygous	45555302
20	39612936	39612937	T	-	5	GENIC	heterozygous	45555304
20	39613149	39613150	C	-	8	GENIC	homozygous	45555305
20	39613419	39613420	G	GTTT	6	GENIC	homozygous	45555306
20	39613898	39613899	C	T	24	GENIC	homozygous	45555308
20	39614109	39614110	C	A	19	GENIC	homozygous	45555309
20	39616337	39616338	C	T	24	GENIC	homozygous	45555310
20	39623235	39623236	A	-	7	GENIC	homozygous	45555311
20	39623536	39623537	G	GTTT	13	GENIC	heterozygous	45555312
20	39624105	39624106	A	ATT	6	GENIC	homozygous	45555314
20	39624339	39624340	A	G	17	GENIC	homozygous	45555315
20	39624495	39624496	T	A	11	GENIC	homozygous	45555316