chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
1	221673875	221673876	T	C	6	GENIC	homozygous	108545019
1	221674126	221674127	G	C	5	GENIC	homozygous	108545021
1	221674408	221674409	G	A	12	GENIC	homozygous	108545023
1	221674631	221674632	C	T	19	GENIC	homozygous	108545025
1	221676450	221676451	G	A	18	GENIC	homozygous	108545027
1	221677431	221677432	T	C	15	GENIC	homozygous	108545029
1	221678393	221678394	A	G	11	GENIC	homozygous	108545031
1	221681844	221681845	G	A	12	GENIC	homozygous	108545033
1	221681869	221681870	T	C	15	GENIC	homozygous	108545035
1	221682384	221682385	A	G	19	GENIC	homozygous	108545037
1	221683624	221683625	G	A	14	GENIC	homozygous	108545039
1	221685458	221685462	AAAC		21	GENIC	homozygous	127485922
1	221685854	221685855	C	T	17	GENIC	possibly homozygous	108545041
1	221687439	221687440	T	C	17	GENIC	homozygous	108545043
1	221687550	221687551	C	T	16	GENIC	homozygous	108545045
1	221688055	221688057	CA		12	GENIC	homozygous	127485923
1	221688060	221688063	GCC		12	GENIC	homozygous	127485924
1	221688772	221688773	G	T	21	GENIC	homozygous	108545047
1	221690296	221690297	G	A	15	GENIC	homozygous	108545049
1	221690342	221690343	A	G	16	GENIC	homozygous	108545051
1	221691100	221691101	C	A	21	GENIC	possibly homozygous	108545053
1	221691169	221691170	A	G	20	GENIC	homozygous	108545055
1	221692311	221692312	C	T	15	GENIC	homozygous	108545057
1	221693460	221693461	A	T	23	GENIC	homozygous	108545059