chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
3	138685926	138685927	C	T	34	GENIC	homozygous	111745452
3	138686378	138686379	C	T	18	GENIC	homozygous	112308034
3	138686423	138686424	T	C	19	GENIC	homozygous	111745454
3	138686713	138686714	A	G	15	GENIC	homozygous	112308036
3	138687698	138687699	T	G	28	GENIC	homozygous	125838702
3	138687753	138687754	T	C	31	GENIC	homozygous	125838703
3	138689984	138689985	T	C	7	GENIC	homozygous	125838706
3	138690272	138690273	T	G	9	GENIC	homozygous	112430756
3	138691255	138691256	T	C	6	GENIC	homozygous	111745464
3	138692897	138692898	T	G	20	GENIC	homozygous	111745470
3	138694390	138694391	A	G	15	GENIC	homozygous	111745472
3	138695150	138695151	T	C	22	GENIC	homozygous	111745474
3	138695820	138695821	G	A	21	GENIC	homozygous	112308038
3	138696570	138696571	T	C	19	GENIC	homozygous	112308040
3	138696666	138696667	T	G	23	GENIC	homozygous	111745480
3	138697911	138697912	A	C	18	GENIC	homozygous	112308042
3	138698095	138698096	T	C	17	GENIC	homozygous	111745482
3	138698348	138698349	T	A	22	GENIC	homozygous	111745484
3	138699361	138699362	A	T	11	GENIC	homozygous	112308044
3	138699567	138699568	A	G	18	GENIC	possibly homozygous	111745496
3	138699579	138699580	C	T	20	GENIC	homozygous	111745498
3	138699708	138699709	G	A	28	GENIC	homozygous	112308046
3	138690210	138690211	G	A	4	GENIC	homozygous	125867986