chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
2	215370415	215370416	T	A	39	GENIC	homozygous	110233162
2	215370734	215370735	C	T	37	GENIC	homozygous	110233163
2	215370778	215370779	G	A	34	GENIC	homozygous	110233164
2	215371055	215371056	C	A	39	GENIC	homozygous	110233165
2	215371244	215371245	A	T	34	GENIC	homozygous	110233166
2	215371489	215371490	A	G	36	GENIC	possibly homozygous	110233167
2	215371509	215371510	T	C	26	GENIC	possibly homozygous	110233168
2	215371573	215371580	GGCCTCT		8	GENIC	homozygous	127735689
2	215371765	215371766	C	T	14	GENIC	possibly homozygous	130897704
2	215371861	215371862	A	G	10	GENIC	homozygous	127836167
2	215371607	215371608	C	G	7	GENIC	homozygous	110818959
2	215371615	215371616	A	G	8	GENIC	homozygous	110818960
2	215371775	215371776	G	A	12	GENIC	heterozygous	127836165
2	215371836	215371837	G	C	10	GENIC	possibly homozygous	127836166
2	215372019	215372020	G	A	12	GENIC	heterozygous	127836168
2	215372051	215372052	G	T	8	GENIC	heterozygous	130897705
2	215372361	215372362	T	C	13	GENIC	heterozygous	134671445
2	215372287	215372288	T	G	8	GENIC	heterozygous	134671443
2	215372291	215372292	A	T	9	GENIC	heterozygous	134671444