chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
19	10668617	10668618	C	A	37	GENIC	homozygous	46059687
19	10669199	10669200	G	GGA	26	GENIC	homozygous	46059688
19	10669549	10669550	C	CAAGGCTGGAGACTGGG	15	GENIC	homozygous	46059689
19	10669705	10669706	T	C	38	GENIC	homozygous	46059690
19	10669977	10669978	G	A	29	GENIC	homozygous	46059691
19	10670242	10670243	G	C	39	GENIC	heterozygous	46059692
19	10670600	10670601	T	G	18	GENIC	homozygous	46059693
19	10670732	10670733	T	G	28	GENIC	homozygous	46059694
19	10670904	10670905	A	G	17	GENIC	homozygous	46059695
19	10671270	10671271	T	-	13	GENIC	homozygous	46059696
19	10671324	10671325	T	C	19	GENIC	heterozygous	46059697
19	10671995	10671996	C	T	33	GENIC	homozygous	46059698
19	10672148	10672149	A	G	28	GENIC	homozygous	46059699
19	10672556	10672557	G	A	10	GENIC	heterozygous	46059700
19	10672600	10672601	G	A	12	GENIC	heterozygous	46271243
19	10672717	10672718	C	T	24	GENIC	homozygous	46059702
19	10673186	10673187	A	G	35	GENIC	homozygous	46059703
19	10673562	10673563	C	T	31	GENIC	homozygous	46059704
19	10674212	10674213	T	C	28	GENIC	homozygous	46059705
19	10674742	10674743	A	G	33	GENIC	homozygous	46059706
19	10674778	10674779	T	C	29	GENIC	homozygous	46059707