chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
13	57175570	57175571	G	A	14	GENIC	possibly homozygous	49766422
13	57176806	57176807	C	T	8	GENIC	homozygous	49766423
13	57176808	57176809	G	A	10	GENIC	homozygous	49766424
13	57177134	57177135	T	C	10	GENIC	possibly homozygous	49766425
13	57177678	57177679	G	A	11	GENIC	homozygous	49766426
13	57178029	57178030	G	GA	13	GENIC	possibly homozygous	49766427
13	57178358	57178359	C	A	15	GENIC	homozygous	49766428
13	57178830	57178831	G	A	11	GENIC	homozygous	49766432
13	57178842	57178843	G	A	9	GENIC	homozygous	49766433
13	57178946	57178947	G	A	21	GENIC	possibly homozygous	49766434
13	57179676	57179677	A	-	3	GENIC	heterozygous	50519261
13	57181098	57181099	G	T	16	GENIC	homozygous	49766436
13	57181212	57181213	C	T	17	GENIC	homozygous	49766438
13	57181323	57181324	T	C	19	GENIC	homozygous	49766439
13	57181512	57181513	G	A	21	GENIC	homozygous	49766440
13	57181909	57181910	A	-	10	GENIC	possibly homozygous	49766441
13	57182181	57182182	A	C	9	GENIC	homozygous	49766442
13	57182271	57182272	A	G	1	GENIC	homozygous	49766443
13	57182525	57182526	C	T	23	GENIC	possibly homozygous	49766444
13	57182669	57182673	ACTT	----	6	GENIC	homozygous	49766445
13	57183896	57183897	C	T	7	GENIC	homozygous	49766447
13	57184338	57184339	C	CTTA	8	GENIC	homozygous	49766448
13	57185478	57185479	T	C	12	GENIC	heterozygous	49766449