chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
10	105123810	105123811	T	C	10	GENIC	homozygous	116836409
10	105125075	105125076	T	C	16	GENIC	heterozygous	116836411
10	105126463	105126464	A	C	4	GENIC	homozygous	126489801
10	105126519	105126520	G	A	26	GENIC	homozygous	116836417
10	105127784	105127785	A	G	16	GENIC	homozygous	116836421
10	105128915	105128916	A	C	13	GENIC	homozygous	116836423
10	105130998	105130999	T	A	25	GENIC	homozygous	116836427
10	105132410	105132411	T	C	19	GENIC	homozygous	116836429
10	105132519	105132520	C	T	26	GENIC	homozygous	116836431
10	105132731	105132732	G	A	22	GENIC	homozygous	116836433
10	105133298	105133299	A	C	23	GENIC	homozygous	116836435
10	105133432	105133433	T	C	14	GENIC	homozygous	116836437
10	105134348	105134349	G	A	16	GENIC	homozygous	116836439
10	105135156	105135157	T	C	4	GENIC	heterozygous	118088172
10	105135222	105135223	T	C	15	GENIC	homozygous	126489802
10	105136355	105136356	T	C	16	GENIC	homozygous	117031665
10	105136798	105136799	T	C	25	GENIC	homozygous	116836441
10	105136992	105136993	G	A	21	GENIC	homozygous	116836443
10	105137511	105137512	T	A	9	GENIC	homozygous	126489803
10	105138177	105138178	A	G	22	GENIC	homozygous	126489804
10	105141347	105141348	A	G	16	GENIC	homozygous	126489805
10	105141528	105141529	T	C	29	GENIC	homozygous	126489806
10	105141616	105141617	G	A	26	GENIC	homozygous	126489807
10	105145388	105145389	G	C	12	GENIC	heterozygous	126489808
10	105146885	105146886	C	T	20	GENIC	homozygous	126489809
10	105148224	105148225	G	T	22	GENIC	homozygous	126489810
10	105148374	105148375	G	A	8	GENIC	homozygous	126489811
10	105148429	105148430	C	T	7	GENIC	homozygous	126489812
10	105148451	105148452	C	A	4	GENIC	homozygous	126489813