chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
15	47489014	47489015	A	T	34	GENIC	homozygous	112680112
15	47493927	47493928	G	T	23	GENIC	homozygous	112680114
15	47566452	47566453	G	T	28	GENIC	homozygous	112501737
15	47566466	47566467	A	T	27	GENIC	homozygous	112501739
15	47645255	47645256	G	T	22	GENIC	heterozygous	112808952
15	47680150	47680151	G	A	28	GENIC	homozygous	112501891
15	47680151	47680152	A	T	28	GENIC	homozygous	112501893
15	47680196	47680197	C	T	37	GENIC	homozygous	112501895
15	47680548	47680549	T	A	23	GENIC	homozygous	112680118
15	47736620	47736621	G	A	22	GENIC	homozygous	112501998
15	47736621	47736622	C	G	21	GENIC	homozygous	112502000
15	47737179	47737180	A	C	25	GENIC	homozygous	112502002
15	47756019	47756020	G	C	28	GENIC	homozygous	112502040
15	47756068	47756069	G	C	22	GENIC	homozygous	112680122
15	47756073	47756074	G	A	22	GENIC	homozygous	112680124
15	47756105	47756106	G	A	21	GENIC	homozygous	112502044
15	47756106	47756107	G	C	21	GENIC	homozygous	112502046
15	47756112	47756113	G	T	24	GENIC	homozygous	112502048
15	47756149	47756150	G	T	25	GENIC	homozygous	112502050
15	47756164	47756165	C	T	26	GENIC	homozygous	112502052
15	47776853	47776854	G	C	6	GENIC	homozygous	112680126
15	47781904	47781905	G	T	29	GENIC	homozygous	112502086
15	47794040	47794041	A	C	14	GENIC	heterozygous	113023820