chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
1	14401779	14401780	A	C	30	GENIC	possibly homozygous	62665726
1	14402196	14402197	A	AT	22	GENIC	heterozygous	62665727
1	14402991	14402992	T	-	20	GENIC	possibly homozygous	62444306
1	14403247	14403248	A	G	27	GENIC	homozygous	60632464
1	14403559	14403560	T	C	29	GENIC	possibly homozygous	60632465
1	14403893	14403894	C	CAA	6	GENIC	heterozygous	60632466
1	14403893	14403894	C	CA	6	GENIC	heterozygous	60632467
1	14405491	14405492	G	GT	10	GENIC	homozygous	62638693
1	14405679	14405680	A	T	12	GENIC	possibly homozygous	62665728
1	14405737	14405738	C	CAA	5	GENIC	heterozygous	62665729
1	14406478	14406479	A	-	18	GENIC	homozygous	60632469
1	14407125	14407126	T	-	17	GENIC	homozygous	60632470
1	14407537	14407538	G	A	26	GENIC	homozygous	62665730
1	14408504	14408505	C	A	15	GENIC	possibly homozygous	62665731
1	14409859	14409860	A	G	28	GENIC	possibly homozygous	60632472
1	14410521	14410522	A	T	5	GENIC	homozygous	62665732
1	14410717	14410718	G	A	14	GENIC	homozygous	62665733
1	14410738	14410739	T	C	11	GENIC	homozygous	60632477
1	14412061	14412062	C	CTTTTGGTTTTGG	23	GENIC	possibly homozygous	60632480
1	14412452	14412453	T	C	20	GENIC	homozygous	60632482
1	14412882	14412883	G	A	30	GENIC	homozygous	62665734
1	14414113	14414114	A	C	32	GENIC	homozygous	60632486
1	14415038	14415039	T	TG	9	GENIC	heterozygous	62479184
1	14416127	14416128	C	T	30	GENIC	possibly homozygous	62665735