chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
20	39612140	39612141	A	G	38	GENIC	homozygous	45555299
20	39612302	39612303	T	TAAA	32	GENIC	homozygous	45555300
20	39612532	39612533	C	T	46	GENIC	homozygous	45555301
20	39612587	39612588	T	C	39	GENIC	homozygous	45555302
20	39612935	39612937	TT	--	36	GENIC	heterozygous	45555303
20	39612936	39612937	T	-	36	GENIC	heterozygous	45555304
20	39613149	39613150	C	-	10	GENIC	homozygous	45555305
20	39613419	39613420	G	GTTT	23	GENIC	heterozygous	45555306
20	39613419	39613420	G	GTT	23	GENIC	heterozygous	45555307
20	39613898	39613899	C	T	39	GENIC	homozygous	45555308
20	39614109	39614110	C	A	49	GENIC	homozygous	45555309
20	39616337	39616338	C	T	48	GENIC	homozygous	45555310
20	39623235	39623236	A	-	8	GENIC	homozygous	45555311
20	39623536	39623537	G	GTTT	24	GENIC	heterozygous	45555312
20	39623536	39623537	G	GTT	24	GENIC	heterozygous	45822763
20	39624105	39624106	A	ATT	11	GENIC	homozygous	45555314
20	39624339	39624340	A	G	19	GENIC	homozygous	45555315
20	39624495	39624496	T	A	40	GENIC	homozygous	45555316