chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
13	109450774	109450775	C	A	12	GENIC	homozygous	114442869
13	109509331	109509332	G	A	28	GENIC	homozygous	114443016
13	109509332	109509333	A	T	27	GENIC	homozygous	114443018
13	109509403	109509404	T	G	18	GENIC	homozygous	114443020
13	109509526	109509527	G	C	14	GENIC	homozygous	114443022
13	109509884	109509885	T	G	15	GENIC	homozygous	114602306
13	109528492	109528493	G	A	28	GENIC	homozygous	114443048
13	109528547	109528548	A	C	21	GENIC	homozygous	114443050
13	109528548	109528549	C	A	21	GENIC	homozygous	114443052
13	109537794	109537795	G	A	22	GENIC	homozygous	114443060
13	109541239	109541240	T	G	28	GENIC	homozygous	114443080
13	109545030	109545031	A	G	19	GENIC	homozygous	114443086
13	109545036	109545037	C	G	21	GENIC	homozygous	114443088
13	109545055	109545056	G	T	25	GENIC	possibly homozygous	114443090
13	109545059	109545060	G	T	24	GENIC	possibly homozygous	114443092
13	109545135	109545136	C	G	7	GENIC	homozygous	114443102
13	109545138	109545139	T	C	7	GENIC	homozygous	114443104
13	109545141	109545142	C	G	8	GENIC	homozygous	114443106
13	109567527	109567528	C	G	18	GENIC	homozygous	114655284
13	109544239	109544240	G	A	20	GENIC	homozygous	114655281
13	109546881	109546882	G	C	7	GENIC	heterozygous	114655282
13	109546882	109546883	T	C	6	GENIC	heterozygous	114655283
13	109578071	109578072	G	T	23	GENIC	homozygous	114602320
13	109578097	109578098	G	A	22	GENIC	homozygous	114602322
13	109578234	109578235	T	C	24	GENIC	homozygous	114443180
13	109582140	109582141	T	C	32	GENIC	homozygous	114443190
13	109582142	109582143	C	T	32	GENIC	homozygous	114443192
13	109582628	109582629	A	C	20	GENIC	homozygous	114443196
13	109582629	109582630	C	A	20	GENIC	homozygous	114443198