chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
19	10674403	10674404	C	A	36	GENIC	homozygous	109634736
19	10675491	10675492	T	C	37	GENIC	homozygous	109634738
19	10675763	10675764	G	A	29	GENIC	homozygous	109634741
19	10676386	10676387	T	G	18	GENIC	homozygous	109764632
19	10676518	10676519	T	G	29	GENIC	homozygous	109634743
19	10676690	10676691	A	G	16	GENIC	homozygous	109634745
19	10677934	10677935	A	G	28	GENIC	homozygous	109634751
19	10678689	10678690	C	T	22	GENIC	homozygous	109634755
19	10679534	10679535	C	T	31	GENIC	homozygous	109634757
19	10680184	10680185	T	C	26	GENIC	homozygous	109634759
19	10680714	10680715	A	G	32	GENIC	homozygous	109634761
19	10680750	10680751	T	C	28	GENIC	homozygous	109634763