chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
20	39612140	39612141	A	G	18	GENIC	possibly homozygous	45555299
20	39612302	39612303	T	TAAA	3	GENIC	homozygous	45555300
20	39612532	39612533	C	T	23	GENIC	possibly homozygous	45555301
20	39612587	39612588	T	C	24	GENIC	possibly homozygous	45555302
20	39613898	39613899	C	T	21	GENIC	homozygous	45555308
20	39614109	39614110	C	A	24	GENIC	homozygous	45555309
20	39616337	39616338	C	T	19	GENIC	possibly homozygous	45555310
20	39623235	39623236	A	-	4	GENIC	heterozygous	45555311
20	39623536	39623537	G	GTT	2	GENIC	heterozygous	45822763
20	39624105	39624106	A	ATT	3	GENIC	heterozygous	45555314
20	39624105	39624106	A	AT	3	GENIC	heterozygous	45822764
20	39624339	39624340	A	G	8	GENIC	homozygous	45555315
20	39624495	39624496	T	A	22	GENIC	homozygous	45555316