chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
13	32053895	32053896	G	A	25	GENIC	homozygous	49705355
13	32055350	32055351	T	C	22	GENIC	possibly homozygous	49705357
13	32055501	32055502	T	C	10	GENIC	homozygous	49705358
13	32055576	32055577	A	AACAT	5	GENIC	heterozygous	49705359
13	32055626	32055630	CACA	----	8	GENIC	homozygous	49705360
13	32056273	32056274	A	G	4	GENIC	heterozygous	49705362
13	32056529	32056530	A	G	16	GENIC	homozygous	50978718
13	32058198	32058199	C	T	13	GENIC	possibly homozygous	49705367
13	32058540	32058541	T	C	8	GENIC	possibly homozygous	49705368
13	32058766	32058767	G	A	6	GENIC	homozygous	49705369
13	32059364	32059365	C	G	23	GENIC	possibly homozygous	49705370
13	32059785	32059786	C	T	17	GENIC	homozygous	49705371
13	32060718	32060719	C	T	20	GENIC	homozygous	50978719
13	32060745	32060746	G	C	17	GENIC	possibly homozygous	49705372
13	32061294	32061295	T	-	8	GENIC	homozygous	49705373
13	32061408	32061409	G	T	12	GENIC	possibly homozygous	49705375
13	32061566	32061567	G	A	5	GENIC	homozygous	49705376
13	32061805	32061806	G	GA	9	GENIC	possibly homozygous	49705377
13	32061808	32061809	G	A	9	GENIC	possibly homozygous	49922253
13	32062124	32062125	C	T	16	GENIC	possibly homozygous	49705378
13	32062297	32062298	C	T	15	GENIC	homozygous	50978720
13	32064034	32064035	C	CA	16	GENIC	homozygous	50978721
13	32069148	32069149	C	T	14	GENIC	possibly homozygous	49705409
13	32069501	32069502	A	AG	1	GENIC	homozygous	49705411
13	32070515	32070516	A	G	8	GENIC	homozygous	49705419
13	32071158	32071159	T	TTTTTTGTTTTG	1	GENIC	homozygous	50978723
13	32072237	32072238	T	C	12	GENIC	homozygous	49922258
13	32072325	32072326	A	C	15	GENIC	possibly homozygous	50978724
13	32072797	32072798	A	T	17	GENIC	homozygous	50978725
13	32072861	32072862	A	T	14	GENIC	homozygous	49922260
13	32073037	32073038	T	C	4	GENIC	homozygous	49922261
13	32073052	32073053	C	A	3	GENIC	homozygous	49922262
13	32073243	32073244	A	G	8	GENIC	possibly homozygous	49922264