chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
10	90521372	90521373	G	GC	21	GENIC	homozygous	51538631
10	90521475	90521476	G	GC	24	GENIC	homozygous	51538634
10	90521495	90521496	T	TC	23	GENIC	homozygous	51538635
10	90522371	90522374	CGG	---	23	GENIC	homozygous	52396537
10	90522496	90522497	C	T	30	GENIC	homozygous	51736877
10	90522541	90522542	A	G	31	GENIC	homozygous	51736879
10	90522619	90522620	C	A	18	GENIC	homozygous	51736881
10	90523318	90523321	TTG	---	38	GENIC	homozygous	52396539
10	90524611	90524612	T	C	31	GENIC	homozygous	51736892
10	90524927	90524928	C	A	23	GENIC	homozygous	52165643
10	90524989	90524990	C	T	36	GENIC	homozygous	52396541
10	90525183	90525184	G	A	18	GENIC	homozygous	52165644
10	90525956	90525958	TG	--	37	GENIC	homozygous	52396543
10	90526022	90526026	GTGA	----	5	GENIC	homozygous	52396545
10	90526087	90526088	G	GA	15	GENIC	homozygous	52396549
10	90526089	90526090	A	ACTCAGTTTGAGATCTGTGAGTGAGCTGAGCCTTCTGGGGACTGGCAGGGATTGGCTCTGCAGATGAGGCC	15	GENIC	homozygous	52396550
10	90526093	90526094	G	T	15	GENIC	homozygous	52396552
10	90529736	90529737	C	T	29	GENIC	homozygous	52396554
10	90531053	90531054	C	T	30	GENIC	homozygous	52396556
10	90531806	90531807	T	C	28	GENIC	homozygous	51736905
10	90532016	90532017	C	G	31	GENIC	homozygous	52396558
10	90532766	90532767	T	C	28	GENIC	homozygous	51736909
10	90532827	90532828	T	G	29	GENIC	homozygous	51736911
10	90533671	90533672	A	G	18	GENIC	homozygous	52165648
10	90533698	90533699	C	T	23	GENIC	homozygous	52396560
10	90534775	90534787	TCTCTCTCTCTC	------------	12	GENIC	heterozygous	52396562
10	90535013	90535014	C	T	20	GENIC	homozygous	52396564
10	90536309	90536310	T	C	28	GENIC	homozygous	51736919
10	90538183	90538184	A	C	30	GENIC	homozygous	51736923