chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
4	37004677	37004678	C		17	GENIC	homozygous	136876895
4	37072163	37072167	CATC		34	GENIC	homozygous	140994864
4	37113526	37113526		GC	23	GENIC	possibly homozygous	140994865
4	37171398	37171399	A	T	15	GENIC	heterozygous	137015493
4	37233166	37233168	GT		20	GENIC	heterozygous	140994866
4	37248486	37248487	A	G	39	GENIC	homozygous	137015625
4	37283286	37283286		AC	11	GENIC	heterozygous	140994867
4	37291882	37291883	G	C	12	GENIC	heterozygous	403096465
4	37190101	37190102	A		26	GENIC	heterozygous	403096445
4	37190101	37190102	A	G	26	GENIC	heterozygous	403096446
4	37291882	37291883	G		12	GENIC	homozygous	403096464
4	37291882	37291883	G	T	12	GENIC	heterozygous	403096466
4	37291884	37291885	G		12	GENIC	homozygous	403096467
4	37291884	37291885	G	C	12	GENIC	heterozygous	403096468
4	37291884	37291885	G	T	12	GENIC	heterozygous	403096469
4	37291886	37291887	G		12	GENIC	homozygous	403096470
4	37291886	37291887	G	C	12	GENIC	heterozygous	403096471
4	37291886	37291887	G	T	12	GENIC	heterozygous	403096472