chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
1	126515807	126515808	A	C	22	GENIC	homozygous	109134443
1	126516158	126516159	T	C	21	GENIC	homozygous	108220039
1	126516398	126516399	T	C	14	GENIC	homozygous	108220041
1	126516417	126516418	C	T	18	GENIC	homozygous	109134445
1	126516771	126516772	G	A	39	GENIC	homozygous	109134447
1	126517692	126517693	T	C	17	GENIC	homozygous	108220047
1	126518073	126518074	C	T	10	GENIC	homozygous	109134449
1	126518943	126518944	T	C	18	GENIC	homozygous	108220053
1	126519380	126519381	T	G	19	GENIC	homozygous	108220057
1	126519771	126519772	A	T	25	GENIC	homozygous	108220059
1	126519995	126519996	T	C	23	GENIC	homozygous	108220060
1	126520362	126520363	A	G	12	GENIC	homozygous	108220064
1	126520423	126520424	G	T	14	GENIC	homozygous	108220066
1	126520504	126520505	C	G	12	GENIC	homozygous	108220068
1	126520530	126520531	C	T	9	GENIC	homozygous	108220070
1	126520541	126520542	A	G	13	GENIC	homozygous	108220072
1	126520555	126520556	T	G	22	GENIC	homozygous	108220074
1	126520670	126520671	T	C	13	GENIC	homozygous	108220076
1	126520688	126520689	G	A	24	GENIC	homozygous	108220078
1	126520755	126520756	T	C	19	GENIC	homozygous	108220080
1	126520818	126520819	T	G	3	GENIC	heterozygous	120671019
1	126520915	126520916	A	G	19	GENIC	homozygous	108220082
1	126521109	126521110	C	T	18	GENIC	homozygous	108220083
1	126521144	126521145	C	T	18	GENIC	homozygous	108220085
1	126521184	126521185	G	A	9	GENIC	homozygous	109134451
1	126521216	126521217	A	C	4	GENIC	homozygous	120473262
1	126521241	126521242	T	C	18	GENIC	homozygous	108220087
1	126521467	126521468	C	G	24	GENIC	homozygous	108220089
1	126521520	126521521	C	T	18	GENIC	heterozygous	108220091
1	126521587	126521588	T	C	10	GENIC	homozygous	108220093
1	126521641	126521642	T	C	13	GENIC	homozygous	108220095
1	126520852	126520853	G	T	10	GENIC	homozygous	109047878