chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
10	106246130	106246131	A	C	34	GENIC	homozygous	116713916
10	106262073	106262074	C	A	11	GENIC	possibly homozygous	116713918
10	106262120	106262121	A	G	3	GENIC	homozygous	116713920
10	106268222	106268223	G	T	18	GENIC	homozygous	118012591
10	106268239	106268240	G	A	6	GENIC	homozygous	118012592
10	106268440	106268441	G	C	18	GENIC	homozygous	116713926
10	106268446	106268447	G	C	19	GENIC	homozygous	118012593
10	106268468	106268469	A	T	23	GENIC	homozygous	117232450
10	106268894	106268895	G	T	31	GENIC	homozygous	118012594
10	106268948	106268949	A	G	27	GENIC	homozygous	117200952
10	106269015	106269016	T	C	39	GENIC	homozygous	116713928
10	106269021	106269022	A	C	42	GENIC	homozygous	116713930
10	106280154	106280155	G	T	16	GENIC	homozygous	118052932
10	106282395	106282396	A	C	34	GENIC	homozygous	117135408
10	106284180	106284181	T	C	30	GENIC	homozygous	116713932
10	106284200	106284201	T	G	24	GENIC	homozygous	118012597
10	106284294	106284295	A	T	10	GENIC	homozygous	118012598
10	106284300	106284301	G	T	11	GENIC	homozygous	118012599