chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
2	250219498	250219499	C	T	25	GENIC	homozygous	110850067
2	250219930	250219931	A	G	33	GENIC	homozygous	110850069
2	250220264	250220265	C	T	38	GENIC	homozygous	110850071
2	250220998	250220999	A	G	23	GENIC	homozygous	110850073
2	250221403	250221404	G	A	20	GENIC	homozygous	110850075
2	250225022	250225023	G	A	32	GENIC	heterozygous	110635490
2	250226766	250226767	G	A	39	GENIC	homozygous	110850078
2	250226983	250226984	G	A	19	GENIC	homozygous	110850080
2	250227699	250227700	G	T	32	GENIC	possibly homozygous	110377652
2	250227831	250227832	G	A	28	GENIC	homozygous	110850082
2	250227885	250227886	C	T	23	GENIC	homozygous	110850083
2	250228000	250228001	C	T	30	GENIC	homozygous	110850085
2	250228803	250228804	G	T	30	GENIC	homozygous	110850087
2	250229526	250229527	A	T	27	GENIC	homozygous	110377654
2	250229531	250229532	A	C	28	GENIC	homozygous	110377656
2	250230182	250230183	C	T	40	GENIC	homozygous	110850089
2	250230539	250230540	A	C	28	GENIC	homozygous	110850090
2	250230871	250230872	A	C	34	GENIC	homozygous	110377658
2	250231273	250231274	C	A	36	GENIC	homozygous	110850092