chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
19	10668617	10668618	C	A	25	GENIC	homozygous	46059687
19	10669199	10669200	G	GGA	23	GENIC	homozygous	46059688
19	10669549	10669550	C	CAAGGCTGGAGACTGGG	23	GENIC	homozygous	46059689
19	10669705	10669706	T	C	26	GENIC	homozygous	46059690
19	10669977	10669978	G	A	26	GENIC	homozygous	46059691
19	10670232	10670233	G	GTGTGTGTGTC	5	GENIC	heterozygous	46458632
19	10670600	10670601	T	G	19	GENIC	homozygous	46059693
19	10670732	10670733	T	G	22	GENIC	homozygous	46059694
19	10670904	10670905	A	G	17	GENIC	homozygous	46059695
19	10671270	10671271	T	-	18	GENIC	homozygous	46059696
19	10671324	10671325	T	C	15	GENIC	possibly homozygous	46059697
19	10671995	10671996	C	T	21	GENIC	homozygous	46059698
19	10672148	10672149	A	G	24	GENIC	homozygous	46059699
19	10672555	10672567	GGGAGAGAGAGA	------------	1	GENIC	homozygous	46458634
19	10672717	10672718	C	T	16	GENIC	homozygous	46059702
19	10673562	10673563	C	T	24	GENIC	homozygous	46059704
19	10674212	10674213	T	C	34	GENIC	homozygous	46059705
19	10674742	10674743	A	G	16	GENIC	homozygous	46059706
19	10674778	10674779	T	C	20	GENIC	homozygous	46059707
19	10670234	10670235	G	GTGTGTGTC	7	GENIC	heterozygous	46507218
19	10672594	10672595	A	-	4	GENIC	homozygous	46507221
19	10672596	10672597	A	G	4	GENIC	homozygous	46507223
19	10672598	10672599	A	G	5	GENIC	homozygous	46507225
19	10670504	10670505	C	CTTTTTTTT	12	GENIC	homozygous	46428089