chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
16	20442349	20442350	C	T	25	GENIC	homozygous	112052893
16	20442579	20442580	C	A	21	GENIC	homozygous	111752812
16	20443715	20443716	A	G	17	GENIC	homozygous	111752814
16	20445302	20445303	A	G	27	GENIC	homozygous	111752818
16	20447972	20447973	A	T	23	GENIC	homozygous	111752822
16	20452295	20452296	C	T	8	GENIC	homozygous	112052894
16	20452354	20452355	T	C	8	GENIC	homozygous	111752828
16	20454454	20454455	C	T	19	GENIC	homozygous	111752832
16	20454710	20454711	C	G	21	GENIC	homozygous	112052895
16	20455203	20455204	A	G	12	GENIC	homozygous	112052896
16	20456462	20456463	G	T	17	GENIC	possibly homozygous	111752836
16	20458946	20458947	C	T	16	GENIC	possibly homozygous	111948673
16	20451687	20451687		G	22	GENIC	homozygous	129340449
16	20456701	20456701		TGCC	5	GENIC	heterozygous	129340450
16	20457838	20457959	GGTCTCGCTTGTTTTTTTTTTTTTTTTTTTTTTTGGTTCTTTTTTTCGGAGCTGGGGACCGAACCCAGGGCCTTGCGCTTCCTAGGTAAGCGCTCTACCACTGTGCTAAATCCCCAGCCCC		2	GENIC	heterozygous	129340451
16	20453113	20453114	G	A	7	GENIC	homozygous	119192775
16	20458479	20458480	C	T	18	GENIC	homozygous	112108007
16	20459251	20459252	T	C	11	GENIC	homozygous	111752838
16	20459531	20459532	G	A	20	GENIC	homozygous	111948675
16	20460072	20460073	A	G	20	GENIC	homozygous	111752840
16	20460126	20460127	T	A	17	GENIC	homozygous	111948677
16	20461444	20461445	G	A	22	GENIC	homozygous	111948679
16	20462132	20462133	C		12	GENIC	homozygous	129340453
16	20462567	20462568	C	T	18	GENIC	homozygous	111948681
16	20462615	20462616	A	T	18	GENIC	homozygous	111752846
16	20459159	20459159		C	10	GENIC	homozygous	131173836
16	20463759	20463760	C		10	GENIC	homozygous	131173837