chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
5	56239388	56239389	T	C	43	GENIC	homozygous	137475207
5	56239585	56239586	A	G	32	GENIC	homozygous	137475208
5	56239799	56239800	C	T	22	GENIC	homozygous	137475209
5	56239923	56239924	T	C	42	GENIC	homozygous	137475210
5	56240026	56240028	GG		40	GENIC	homozygous	137309809
5	56240045	56240046	G	T	33	GENIC	homozygous	137475211
5	56240047	56240048	A	G	40	GENIC	homozygous	137475212
5	56240117	56240118	A	G	46	GENIC	homozygous	137475213
5	56241131	56241132	G	T	43	GENIC	possibly homozygous	137475214
5	56241295	56241296	C	T	42	GENIC	homozygous	137475215
5	56241589	56241590	T	C	45	GENIC	homozygous	137475216
5	56241633	56241634	C	T	37	GENIC	homozygous	137475217
5	56242050	56242051	T	C	40	GENIC	homozygous	137475218
5	56242188	56242189	A	G	37	GENIC	homozygous	137475219
5	56242532	56242533	C	T	36	GENIC	homozygous	137475220
5	56242640	56242641	A	C	43	GENIC	homozygous	137475221
5	56242934	56242934		C	37	GENIC	homozygous	137309810
5	56242936	56242937	T	G	38	GENIC	homozygous	137475222
5	56243159	56243160	G	T	41	GENIC	possibly homozygous	137475223
5	56243324	56243325	T	C	40	GENIC	possibly homozygous	137475224
5	56243468	56243469	T	C	33	GENIC	homozygous	137475225
5	56243610	56243612	TC		31	GENIC	homozygous	137309811
5	56243612	56243613	G	A	32	GENIC	homozygous	137475226
5	56243615	56243618	TGT		32	GENIC	homozygous	137309812
5	56244139	56244140	C	G	44	GENIC	homozygous	137475227
5	56244198	56244199	C	T	52	GENIC	homozygous	137475228
5	56244337	56244338	C	T	56	GENIC	homozygous	137475229
5	56244354	56244355	T	A	57	GENIC	homozygous	137475230