chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
10	10726252	10726253	C	A	18	GENIC	homozygous	116493625
10	10727385	10727386	A	G	16	GENIC	homozygous	116493627
10	10732436	10732437	T	C	18	GENIC	homozygous	116493631
10	10733457	10733458	C	A	27	GENIC	homozygous	116734058
10	10733744	10733745	T	A	23	GENIC	homozygous	116734059
10	10734366	10734367	G	A	12	GENIC	homozygous	116734060
10	10734368	10734369	T	A	14	GENIC	homozygous	116734061
10	10740094	10740095	A	G	16	GENIC	homozygous	116734062
10	10743407	10743408	G	A	15	GENIC	homozygous	116493637
10	10744713	10744714	C	G	24	GENIC	homozygous	116734064
10	10744957	10744958	A	G	9	GENIC	homozygous	116734065
10	10745033	10745034	T	C	8	GENIC	homozygous	116734066
10	10746140	10746141	C	T	21	GENIC	homozygous	116734067
10	10750923	10750924	G	A	22	GENIC	homozygous	116734068
10	10753203	10753204	G	A	20	GENIC	homozygous	116734069
10	10753356	10753357	A	G	18	GENIC	homozygous	116734070
10	10753422	10753423	T	A	8	GENIC	homozygous	116734071
10	10753425	10753426	C	G	9	GENIC	homozygous	116734072
10	10754649	10754650	C	G	11	GENIC	homozygous	116734073
10	10756008	10756009	G	A	20	GENIC	homozygous	116493645
10	10757442	10757443	G	C	19	GENIC	homozygous	116493649
10	10758674	10758675	T	C	16	GENIC	homozygous	116734074
10	10758737	10758738	C	G	21	GENIC	homozygous	116493651