chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
10	106829688	106829689	T	C	12	GENIC	homozygous	116840508
10	106829788	106829789	T	C	18	GENIC	homozygous	116840510
10	106829885	106829886	C	T	13	GENIC	homozygous	116840512
10	106830348	106830349	C	T	17	GENIC	homozygous	116840514
10	106830791	106830792	G	A	10	GENIC	homozygous	116840516
10	106830983	106830984	G	A	20	GENIC	homozygous	116840518
10	106831498	106831499	A	C	14	GENIC	homozygous	116840520
10	106831744	106831745	A	G	29	GENIC	homozygous	116840522
10	106832135	106832136	C	T	28	GENIC	homozygous	116840526
10	106832874	106832875	C	T	20	GENIC	homozygous	116840528
10	106834834	106834835	C	A	30	GENIC	homozygous	116840532
10	106834939	106834940	C	A	17	GENIC	homozygous	116840534
10	106837221	106837222	G	C	17	GENIC	homozygous	117033515
10	106838790	106838791	T	C	27	GENIC	homozygous	116840540
10	106838822	106838823	G	A	24	GENIC	homozygous	117033517
10	106838904	106838905	A	G	29	GENIC	homozygous	116840542
10	106839879	106839880	T	C	14	GENIC	homozygous	116840550
10	106839991	106839992	G	A	19	GENIC	homozygous	117033519
10	106841547	106841548	C	T	18	GENIC	homozygous	117033521
10	106842900	106842901	C	T	14	GENIC	homozygous	117033523
10	106843166	106843167	C	G	16	GENIC	homozygous	117033525
10	106843854	106843855	C	T	15	GENIC	homozygous	117261248
10	106843855	106843856	A	G	15	GENIC	homozygous	117261250
10	106843916	106843917	T	C	13	GENIC	homozygous	117261252
10	106844212	106844213	A	G	15	GENIC	homozygous	117033527
10	106843502	106843503	C	T	20	GENIC	possibly homozygous	117392698