chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
19	10668617	10668618	C	A	19	GENIC	homozygous	46059687
19	10669199	10669200	G	GGA	21	GENIC	homozygous	46059688
19	10669549	10669550	C	CAAGGCTGGAGACTGGG	13	GENIC	homozygous	46059689
19	10669705	10669706	T	C	19	GENIC	homozygous	46059690
19	10670072	10670073	A	G	23	GENIC	homozygous	46788895
19	10670228	10670229	T	TTCTGTGTGTGTG	4	GENIC	heterozygous	46788897
19	10670504	10670505	C	CTTTTTTTT	6	GENIC	homozygous	46428089
19	10670600	10670601	T	G	20	GENIC	homozygous	46059693
19	10670732	10670733	T	G	21	GENIC	possibly homozygous	46059694
19	10670904	10670905	A	G	16	GENIC	homozygous	46059695
19	10671270	10671271	T	-	14	GENIC	homozygous	46059696
19	10671355	10671356	C	T	6	GENIC	homozygous	46546797
19	10672148	10672149	A	G	24	GENIC	homozygous	46059699
19	10672555	10672567	GGGAGAGAGAGA	------------	1	GENIC	homozygous	46458634
19	10673328	10673329	T	-	26	GENIC	homozygous	46788899
19	10673562	10673563	C	T	9	GENIC	homozygous	46059704
19	10674212	10674213	T	C	21	GENIC	homozygous	46059705
19	10674742	10674743	A	G	12	GENIC	homozygous	46059706
19	10674778	10674779	T	C	17	GENIC	homozygous	46059707
19	10674905	10674906	C	T	15	GENIC	homozygous	46486236