chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
10	94355635	94355636	A	G	17	GENIC	homozygous	116826350
10	94357906	94357907	G	A	19	GENIC	homozygous	116954859
10	94357996	94357997	C	T	23	GENIC	homozygous	116954861
10	94360477	94360478	C	T	17	GENIC	homozygous	116685060
10	94360597	94360598	C	A	15	GENIC	homozygous	116954863
10	94361306	94361307	C	A	15	GENIC	homozygous	116826352
10	94362086	94362087	C	T	19	GENIC	homozygous	116826356
10	94362196	94362197	A	T	19	GENIC	homozygous	116685064
10	94362617	94362618	T	G	17	GENIC	homozygous	116685068
10	94362686	94362687	T	C	26	GENIC	homozygous	116826360
10	94363354	94363355	C	A	26	GENIC	homozygous	116826362
10	94363481	94363482	A	G	17	GENIC	homozygous	116685072
10	94364406	94364407	A	C	30	GENIC	heterozygous	117259170
10	94365561	94365562	A	C	40	GENIC	homozygous	116826366
10	94365715	94365716	T	C	29	GENIC	homozygous	116826368
10	94365944	94365945	G	A	24	GENIC	homozygous	116954865
10	94367244	94367245	C	A	27	GENIC	homozygous	116954867
10	94368125	94368126	G	A	22	GENIC	homozygous	116685082
10	94368384	94368385	G	C	17	GENIC	homozygous	116685084