chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
2	215370415	215370416	T	A	40	GENIC	homozygous	110233162
2	215370734	215370735	C	T	32	GENIC	homozygous	110233163
2	215370778	215370779	G	A	34	GENIC	homozygous	110233164
2	215371055	215371056	C	A	20	GENIC	homozygous	110233165
2	215371244	215371245	A	T	42	GENIC	homozygous	110233166
2	215371489	215371490	A	G	25	GENIC	homozygous	110233167
2	215371509	215371510	T	C	18	GENIC	homozygous	110233168
2	215371573	215371580	GGCCTCT		7	GENIC	homozygous	127735689
2	215371765	215371766	C	T	20	GENIC	possibly homozygous	130897704
2	215371861	215371862	A	G	11	GENIC	homozygous	127836167
2	215371607	215371608	C	G	4	GENIC	homozygous	110818959
2	215371615	215371616	A	G	4	GENIC	homozygous	110818960
2	215371775	215371776	G	A	20	GENIC	possibly homozygous	127836165
2	215371836	215371837	G	C	11	GENIC	possibly homozygous	127836166
2	215371999	215372000	A		12	GENIC	heterozygous	127735690
2	215372019	215372020	G	A	11	GENIC	heterozygous	127836168
2	215372051	215372052	G	T	8	GENIC	heterozygous	130897705
2	215372331	215372332	C	A	9	GENIC	heterozygous	131835210