chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
2	30545293	30545294	G	C	22	GENIC	heterozygous	109674978
2	30545297	30545298	C	T	22	GENIC	heterozygous	110501353
2	30545399	30545400	G	T	26	GENIC	heterozygous	109674982
2	30570441	30570442	C	T	25	GENIC	homozygous	111233147
2	30570564	30570565	G	C	28	GENIC	homozygous	111098366
2	30570904	30570905	T	C	19	GENIC	homozygous	110501416
2	30571148	30571149	G	A	24	GENIC	homozygous	110501418
2	30571266	30571268	TC		13	GENIC	heterozygous	132275518
2	30572334	30572335	A	G	5	GENIC	homozygous	110501422
2	30573060	30573061	G	T	28	GENIC	homozygous	110501424
2	30574201	30574202	G	A	18	GENIC	homozygous	110501430
2	30574540	30574540		GTTCTGGAACTCAC	14	GENIC	homozygous	130244047
2	30569757	30569758	A		11	GENIC	homozygous	130244043
2	30571591	30571591		A	19	GENIC	homozygous	130244045
2	30572172	30572289	GAAAGCAGGAATAAGGGGTTGGGGATTTAGCTCAGTGGTAGAGCGCTTGCCTAGCAAGCGCAAGGCCCTGGGTTCGGTCCCCAGCTCCGAAAAAAAAAAAAAAAAAAAAAAGATTAA		5	GENIC	heterozygous	130244046
2	30574632	30574633	G	T	14	GENIC	homozygous	110501432
2	30575049	30575051	CG		10	GENIC	homozygous	130244048
2	30575164	30575164		G	4	GENIC	homozygous	130244049
2	30577051	30577052	A	T	24	GENIC	homozygous	109675209
2	30577198	30577199	G	A	20	GENIC	homozygous	111098372
2	30577118	30577119	C	G	19	GENIC	homozygous	120165318
2	30575670	30575671	C	A	11	GENIC	homozygous	120165316