chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
19	10674403	10674404	C	A	26	GENIC	homozygous	109634736
19	10675491	10675492	T	C	23	GENIC	homozygous	109634738
19	10675858	10675859	A	G	32	GENIC	possibly homozygous	110076371
19	10676386	10676387	T	G	22	GENIC	homozygous	109764632
19	10676518	10676519	T	G	24	GENIC	homozygous	109634743
19	10676690	10676691	A	G	26	GENIC	homozygous	109634745
19	10677934	10677935	A	G	27	GENIC	homozygous	109634751
19	10679534	10679535	C	T	16	GENIC	homozygous	109634757
19	10680184	10680185	T	C	32	GENIC	homozygous	109634759
19	10680714	10680715	A	G	29	GENIC	homozygous	109634761
19	10680750	10680751	T	C	25	GENIC	homozygous	109634763
19	10680877	10680878	C	T	21	GENIC	possibly homozygous	110076373