chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
1	126516158	126516159	T	C	28	GENIC	homozygous	108220039
1	126516398	126516399	T	C	24	GENIC	homozygous	108220041
1	126517261	126517262	C	T	36	GENIC	homozygous	108220043
1	126517692	126517693	T	C	32	GENIC	homozygous	108220047
1	126517804	126517805	G	A	26	GENIC	homozygous	108220049
1	126517872	126517873	G	A	25	GENIC	homozygous	108926257
1	126518001	126518002	G	A	30	GENIC	homozygous	108926258
1	126518683	126518684	G	A	38	GENIC	homozygous	108220051
1	126518943	126518944	T	C	21	GENIC	homozygous	108220053
1	126518986	126518987	A	T	23	GENIC	homozygous	108220055
1	126519380	126519381	T	G	14	GENIC	homozygous	108220057
1	126519771	126519772	A	T	28	GENIC	homozygous	108220059
1	126519995	126519996	T	C	13	GENIC	homozygous	108220060
1	126520064	126520065	C	G	23	GENIC	homozygous	108220062
1	126520362	126520363	A	G	18	GENIC	homozygous	108220064
1	126520423	126520424	G	T	13	GENIC	homozygous	108220066
1	126520504	126520505	C	G	14	GENIC	homozygous	108220068
1	126520530	126520531	C	T	20	GENIC	homozygous	108220070
1	126520541	126520542	A	G	19	GENIC	homozygous	108220072
1	126520555	126520556	T	G	24	GENIC	homozygous	108220074
1	126520670	126520671	T	C	27	GENIC	homozygous	108220076
1	126520688	126520689	G	A	25	GENIC	homozygous	108220078
1	126520755	126520756	T	C	25	GENIC	homozygous	108220080
1	126520915	126520916	A	G	20	GENIC	homozygous	108220082
1	126521109	126521110	C	T	26	GENIC	homozygous	108220083
1	126521144	126521145	C	T	33	GENIC	homozygous	108220085
1	126521216	126521217	A	C	24	GENIC	homozygous	120473262
1	126521241	126521242	T	C	22	GENIC	homozygous	108220087
1	126521467	126521468	C	G	25	GENIC	homozygous	108220089
1	126521587	126521588	T	C	22	GENIC	homozygous	108220093
1	126521641	126521642	T	C	27	GENIC	homozygous	108220095